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The novel HLA‐C*01:38 variant allele differs from the closest allele C*01:02:01 by a single nucleotide change at coding sequence (CDS) nt 430 G>A (codon 120 GGC>AGC) in exon 3, which causes an amino acid change Gly120Ser.
The novel human leukocyte antigen (HLA)‐Cw*075602 variant allele differs from the closest allele Cw*07020101 by a single nucleotide change at genomic DNA nt 473 G > C (CDS nt 343 G > C , codon 91 GGG > CGG ) in exon 2, which results in an amino acid change Gly91Arg.
A novel HLA‐Cw*0624 variant allele differs from the closest allele Cw*06020101 by single nucleotide change at genomic nt 923 T>C (CDS nt 547 T>C, codon 159 TAC>CAC) in exon 3, which results in an amino acid change Tyr159His.
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