Canonical Allele Identifier: CA363314699
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v3: 6-31357041-T-G
gnomAD v4: 6-31357041-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357041T>G , CM000668.2:g.31357041T>G GRCh38
NC_000006.11:g.31324818T>G , CM000668.1:g.31324818T>G GRCh37
NC_000006.10:g.31432797T>G NCBI36
NG_023187.1:g.5172A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1546+45A>C
ENST00000481849.6:n.1546+45A>C
ENST00000497377.6:n.1546+45A>C
ENST00000640094.2:c.73+45A>C ENSP00000491275.2:n.73+45A>C
ENST00000696558.1:c.73+45A>C ENSP00000512716.1:n.73+45A>C
ENST00000696559.1:c.73+45A>C ENSP00000512717.1:n.73+45A>C
ENST00000696560.1:c.73+45A>C ENSP00000512718.1:n.73+45A>C
ENST00000696561.1:c.73+45A>C ENSP00000512719.1:n.73+45A>C
ENST00000696562.1:c.73+45A>C ENSP00000512720.1:n.73+45A>C
ENST00000412585.7:c.73+45A>C MANE Select ENSP00000399168.2:n.73+45A>C
ENST00000412585.6:c.73+45A>C ENSP00000399168.2:n.73+45A>C
ENST00000434333.1:c.23A>C ENSP00000405931.1:p.Glu8Ala
ENST00000498007.1:n.94+45A>C
ENST00000603274.1:n.395T>G
NM_005514.6:c.73+45A>C NP_005505.2:n.73+45A>C
XM_011514556.1:c.23A>C XP_011512858.1:p.Glu8Ala
XM_011514557.1:c.73+45A>C XP_011512859.1:n.73+45A>C
XR_926175.1:n.83+45A>C
NM_005514.7:c.73+45A>C NP_005505.2:n.73+45A>C
NM_005514.8:c.73+45A>C MANE Select NP_005505.2:n.73+45A>C