Canonical Allele Identifier: CA1619116771
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1767485222

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359303T>C , CM000668.2:g.31359303T>C GRCh38
NC_000006.11:g.31327080T>C , CM000668.1:g.31327080T>C GRCh37
NC_000006.10:g.31435059T>C NCBI36
NG_023187.1:g.2910A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1271-1622A>G
ENST00000481849.6:n.1271-1622A>G
ENST00000497377.6:n.1271-1622A>G
ENST00000696559.1:c.-203-1622A>G ENSP00000512717.1:n.-203-1622A>G
ENST00000696560.1:c.-203-1622A>G ENSP00000512718.1:n.-203-1622A>G
ENST00000696561.1:c.-203-1622A>G ENSP00000512719.1:n.-203-1622A>G
ENST00000696562.1:c.-135-2010A>G ENSP00000512720.1:n.-135-2010A>G