Canonical Allele Identifier: CA1087460180

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766693056
• gnomAD v3: 6-31354401-A-C
• gnomAD v4: 6-31354401-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354401A>C , CM000668.2:g.31354401A>C	GRCh38
NC_000006.11:g.31322178A>C , CM000668.1:g.31322178A>C	GRCh37
NC_000006.10:g.31430157A>C	NCBI36
NG_023187.1:g.7812T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3140+78T>G
ENST00000481849.6:n.3100+78T>G
ENST00000497377.6:n.3007+78T>G
ENST00000696558.1:c.1162+78T>G	ENSP00000512716.1:n.1162+78T>G
ENST00000696559.1:c.*4+78T>G	ENSP00000512717.1:n.*4+78T>G
ENST00000696560.1:c.*4+78T>G	ENSP00000512718.1:n.*4+78T>G
ENST00000696561.1:c.*4+78T>G	ENSP00000512719.1:n.*4+78T>G
ENST00000696562.1:c.*4+78T>G	ENSP00000512720.1:n.*4+78T>G
ENST00000412585.7:c.*4+78T>G MANE Select	ENSP00000399168.2:n.*4+78T>G
ENST00000412585.6:c.*4+78T>G	ENSP00000399168.2:n.*4+78T>G
ENST00000481849.5:n.328+78T>G
ENST00000497377.5:n.492+78T>G
NM_005514.6:c.*4+78T>G	NP_005505.2:n.*4+78T>G
XM_011514556.1:c.*4+78T>G	XP_011512858.1:n.*4+78T>G
XM_011514557.1:c.*4+78T>G	XP_011512859.1:n.*4+78T>G
XR_926175.1:n.1532+78T>G
NM_005514.7:c.*4+78T>G	NP_005505.2:n.*4+78T>G
NM_005514.8:c.*4+78T>G MANE Select	NP_005505.2:n.*4+78T>G