Canonical Allele Identifier: CA1619116790
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1767486699

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359335dup , CM000668.2:g.31359335dup GRCh38
NC_000006.11:g.31327112dup , CM000668.1:g.31327112dup GRCh37
NC_000006.10:g.31435091dup NCBI36
NG_023187.1:g.2878dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1271-1654dup
ENST00000481849.6:n.1271-1654dup
ENST00000497377.6:n.1271-1654dup
ENST00000696559.1:c.-203-1654dup ENSP00000512717.1:n.-203-1654dup
ENST00000696560.1:c.-203-1654dup ENSP00000512718.1:n.-203-1654dup
ENST00000696561.1:c.-203-1654dup ENSP00000512719.1:n.-203-1654dup
ENST00000696562.1:c.-135-2042dup ENSP00000512720.1:n.-135-2042dup