Canonical Allele Identifier: CA2677954610

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354968-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354968G>C , CM000668.2:g.31354968G>C	GRCh38
NC_000006.11:g.31322745G>C , CM000668.1:g.31322745G>C	GRCh37
NC_000006.10:g.31430724G>C	NCBI36
NG_023187.1:g.7245C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+139C>G
ENST00000481849.6:n.2717C>G
ENST00000497377.6:n.2624C>G
ENST00000640094.2:c.896-303C>G	ENSP00000491275.2:n.896-303C>G
ENST00000696558.1:c.1081+139C>G	ENSP00000512716.1:n.1081+139C>G
ENST00000696559.1:c.1012+139C>G	ENSP00000512717.1:n.1012+139C>G
ENST00000696560.1:c.1012+139C>G	ENSP00000512718.1:n.1012+139C>G
ENST00000696561.1:c.1012+139C>G	ENSP00000512719.1:n.1012+139C>G
ENST00000696562.1:c.1012+139C>G	ENSP00000512720.1:n.1012+139C>G
ENST00000412585.7:c.1012+139C>G MANE Select	ENSP00000399168.2:n.1012+139C>G
ENST00000640094.1:c.89-303C>G	ENSP00000491275.1:n.89-303C>G
ENST00000412585.6:c.1012+139C>G	ENSP00000399168.2:n.1012+139C>G
ENST00000497377.5:n.109C>G
NM_005514.6:c.1012+139C>G	NP_005505.2:n.1012+139C>G
XM_011514556.1:c.1045+139C>G	XP_011512858.1:n.1045+139C>G
XM_011514557.1:c.896-303C>G	XP_011512859.1:n.896-303C>G
XR_926175.1:n.1451+139C>G
NM_005514.7:c.1012+139C>G	NP_005505.2:n.1012+139C>G
NM_005514.8:c.1012+139C>G MANE Select	NP_005505.2:n.1012+139C>G