Canonical Allele Identifier: CA2677953252

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354233-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354233A>C , CM000668.2:g.31354233A>C	GRCh38
NC_000006.11:g.31322010A>C , CM000668.1:g.31322010A>C	GRCh37
NC_000006.10:g.31429989A>C	NCBI36
NG_023187.1:g.7980T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3204T>G
ENST00000481849.6:n.3164T>G
ENST00000497377.6:n.3071T>G
ENST00000696558.1:c.1226T>G	ENSP00000512716.1:n.1226T>G
ENST00000696559.1:c.*68T>G	ENSP00000512717.1:n.*68T>G
ENST00000696560.1:c.*68T>G	ENSP00000512718.1:n.*68T>G
ENST00000696561.1:c.*68T>G	ENSP00000512719.1:n.*68T>G
ENST00000696562.1:c.*68T>G	ENSP00000512720.1:n.*68T>G
ENST00000412585.7:c.*68T>G MANE Select	ENSP00000399168.2:n.*68T>G
ENST00000412585.6:c.*68T>G	ENSP00000399168.2:n.*68T>G
ENST00000481849.5:n.392T>G
ENST00000497377.5:n.556T>G
NM_005514.6:c.*68T>G	NP_005505.2:n.*68T>G
XM_011514556.1:c.*68T>G	XP_011512858.1:n.*68T>G
XM_011514557.1:c.*68T>G	XP_011512859.1:n.*68T>G
XR_926175.1:n.1596T>G
NM_005514.7:c.*68T>G	NP_005505.2:n.*68T>G
NM_005514.8:c.*68T>G MANE Select	NP_005505.2:n.*68T>G