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May 26, 2026Transfusion

Identification of a novel A allele with a c. 610G >A variation on the ABO*A1.02 allele

Qian Chen Yaqing Zhang Xiaoqiang Wu Kaokao Zhu Zengqiang Feng Zhenhong Liang Qiuping Tang

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Key Points

This research aims to identify and characterize a new allele variation within the ABO gene system.
Data was analyzed and made available through NCBI.
Reference number PX935910 is provided for tracking findings.
The novel A allele with c.610G>A variation is identified in the ABO*A1.02 allele.
Data supporting these findings is openly accessible for further research.

Implication

Investigation identifies a new A allele variation in ABO genetic markers, suggesting potential implications for blood type genetics.

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Cite This Study

Chen et al. (2026) studied this question.

synapsesocial.com/papers/6a192d65fab5b468c4416377 https://doi.org/10.1111/trf.70281

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Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Identification of a novel A allele with a c.<scp>421T</scp>>C variant on the <i>ABO*A1.02</i> allele in a Chinese individual2024 · 1 citations
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3Identification of a novel A allele with a c.374 + 3_374 + <scp>6delAAGT</scp> splicing variant in a Chinese individualOriginal Research · 2026
4Identification of a novel <i>A</i> allele with a nucleotide deletion c.<scp>198delG</scp> in the <i>ABO</i> gene associated with A<sub>el</sub> phenotype2024
5Identification of a novel O allele with c.<scp>777C</scp>>G on an <i>ABO</i>*<i>O.01.02</i> background2024 · 1 citations

Identification of a novel c.<scp>77T</scp>>G mutation on the ABO*B.01 allele associated with a B subtype2024
Novel intron 1 variant c.28+ <scp>5808C</scp> >T on an <i>ABO*A1.01</i> background is associated with an <scp> A <sub>3</sub> </scp> phenotype2026
A Rare Variant <i>c.1024A&gt;C</i> in the <i>ABO*A1.02</i> Allele Was Associated with an A<sub>el</sub> Phenotype2024
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