Genomic Confirmation of HLA‐C*12:68 by Next Generation Sequencing

Key Points

• The aim is to confirm the presence of the HLA-C*12:68 variant using advanced sequencing technology.
• Next generation sequencing was employed for genomic analysis.
• Focus was on identifying nucleotide substitutions in HLA genes.
• Characterization involved examining codon 62 in exon 2.
• HLA-C*12:68 was confirmed with a specific nucleotide substitution identified at codon 62.
• The study efficiently utilized next generation sequencing to detect the genetic variant.