Canonical Allele Identifier: CA2677952673

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31353887-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353887A>C , CM000668.2:g.31353887A>C	GRCh38
NC_000006.11:g.31321664A>C , CM000668.1:g.31321664A>C	GRCh37
NC_000006.10:g.31429643A>C	NCBI36
NG_023187.1:g.8326T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481849.6:n.3510T>G
ENST00000497377.6:n.3417T>G
ENST00000696558.1:c.1572T>G	ENSP00000512716.1:n.1572T>G
ENST00000696559.1:c.*414T>G	ENSP00000512717.1:n.*414T>G
ENST00000696560.1:c.*414T>G	ENSP00000512718.1:n.*414T>G
ENST00000696561.1:c.*414T>G	ENSP00000512719.1:n.*414T>G
ENST00000696562.1:c.*414T>G	ENSP00000512720.1:n.*414T>G
ENST00000412585.7:c.*414T>G MANE Select	ENSP00000399168.2:n.*414T>G
ENST00000412585.6:c.*414T>G	ENSP00000399168.2:n.*414T>G
ENST00000481849.5:n.738T>G
ENST00000497377.5:n.902T>G
NM_005514.6:c.*414T>G	NP_005505.2:n.*414T>G
XM_011514556.1:c.*414T>G	XP_011512858.1:n.*414T>G
XM_011514557.1:c.*414T>G	XP_011512859.1:n.*414T>G
XR_926175.1:n.1942T>G
NM_005514.7:c.*414T>G	NP_005505.2:n.*414T>G
NM_005514.8:c.*414T>G MANE Select	NP_005505.2:n.*414T>G