Canonical Allele Identifier: CA1087447514
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1767485077
gnomAD v3: 6-31359302-G-T
gnomAD v4: 6-31359302-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359302G>T , CM000668.2:g.31359302G>T GRCh38
NC_000006.11:g.31327079G>T , CM000668.1:g.31327079G>T GRCh37
NC_000006.10:g.31435058G>T NCBI36
NG_023187.1:g.2911C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1271-1621C>A
ENST00000481849.6:n.1271-1621C>A
ENST00000497377.6:n.1271-1621C>A
ENST00000696559.1:c.-203-1621C>A ENSP00000512717.1:n.-203-1621C>A
ENST00000696560.1:c.-203-1621C>A ENSP00000512718.1:n.-203-1621C>A
ENST00000696561.1:c.-203-1621C>A ENSP00000512719.1:n.-203-1621C>A
ENST00000696562.1:c.-135-2009C>A ENSP00000512720.1:n.-135-2009C>A