Canonical Allele Identifier: CA3712010
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs114038515
gnomAD v2: 6-31324941-C-T
gnomAD v3: 6-31357164-C-T
gnomAD v4: 6-31357164-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357164C>T , CM000668.2:g.31357164C>T GRCh38
NC_000006.11:g.31324941C>T , CM000668.1:g.31324941C>T GRCh37
NC_000006.10:g.31432920C>T NCBI36
NG_023187.1:g.5049G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1468G>A
ENST00000481849.6:n.1468G>A
ENST00000497377.6:n.1468G>A
ENST00000696559.1:c.-6G>A ENSP00000512717.1:n.-6G>A
ENST00000696560.1:c.-6G>A ENSP00000512718.1:n.-6G>A
ENST00000696561.1:c.-6G>A ENSP00000512719.1:n.-6G>A
ENST00000696562.1:c.-6G>A ENSP00000512720.1:n.-6G>A
ENST00000412585.7:c.-6G>A MANE Select ENSP00000399168.2:n.-6G>A
ENST00000412585.6:c.-6G>A ENSP00000399168.2:n.-6G>A
ENST00000434333.1:c.-101G>A ENSP00000405931.1:n.-101G>A
ENST00000498007.1:n.16G>A
ENST00000603274.1:n.518C>T
NM_005514.6:c.-6G>A NP_005505.2:n.-6G>A
XM_011514557.1:c.-6G>A XP_011512859.1:n.-6G>A
XR_926175.1:n.5G>A
NM_005514.7:c.-6G>A NP_005505.2:n.-6G>A
NM_005514.8:c.-6G>A MANE Select NP_005505.2:n.-6G>A