Canonical Allele Identifier: CA2677954759

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355051-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355051T>G , CM000668.2:g.31355051T>G	GRCh38
NC_000006.11:g.31322828T>G , CM000668.1:g.31322828T>G	GRCh37
NC_000006.10:g.31430807T>G	NCBI36
NG_023187.1:g.7162A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+56A>C
ENST00000481849.6:n.2634A>C
ENST00000497377.6:n.2541A>C
ENST00000640094.2:c.895+266A>C	ENSP00000491275.2:n.895+266A>C
ENST00000696558.1:c.1081+56A>C	ENSP00000512716.1:n.1081+56A>C
ENST00000696559.1:c.1012+56A>C	ENSP00000512717.1:n.1012+56A>C
ENST00000696560.1:c.1012+56A>C	ENSP00000512718.1:n.1012+56A>C
ENST00000696561.1:c.1012+56A>C	ENSP00000512719.1:n.1012+56A>C
ENST00000696562.1:c.1012+56A>C	ENSP00000512720.1:n.1012+56A>C
ENST00000412585.7:c.1012+56A>C MANE Select	ENSP00000399168.2:n.1012+56A>C
ENST00000640094.1:c.88+266A>C	ENSP00000491275.1:n.88+266A>C
ENST00000412585.6:c.1012+56A>C	ENSP00000399168.2:n.1012+56A>C
ENST00000497377.5:n.26A>C
NM_005514.6:c.1012+56A>C	NP_005505.2:n.1012+56A>C
XM_011514556.1:c.1045+56A>C	XP_011512858.1:n.1045+56A>C
XM_011514557.1:c.895+266A>C	XP_011512859.1:n.895+266A>C
XR_926175.1:n.1451+56A>C
NM_005514.7:c.1012+56A>C	NP_005505.2:n.1012+56A>C
NM_005514.8:c.1012+56A>C MANE Select	NP_005505.2:n.1012+56A>C