Canonical Allele Identifier: CA2580592239
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359287T>G , CM000668.2:g.31359287T>G GRCh38
NC_000006.11:g.31327064T>G , CM000668.1:g.31327064T>G GRCh37
NC_000006.10:g.31435043T>G NCBI36
NG_023187.1:g.2926A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1271-1606A>C
ENST00000481849.6:n.1271-1606A>C
ENST00000497377.6:n.1271-1606A>C
ENST00000696559.1:c.-203-1606A>C ENSP00000512717.1:n.-203-1606A>C
ENST00000696560.1:c.-203-1606A>C ENSP00000512718.1:n.-203-1606A>C
ENST00000696561.1:c.-203-1606A>C ENSP00000512719.1:n.-203-1606A>C
ENST00000696562.1:c.-135-1994A>C ENSP00000512720.1:n.-135-1994A>C