Canonical Allele Identifier: CA2677952915

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354032-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354032A>C , CM000668.2:g.31354032A>C	GRCh38
NC_000006.11:g.31321809A>C , CM000668.1:g.31321809A>C	GRCh37
NC_000006.10:g.31429788A>C	NCBI36
NG_023187.1:g.8181T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3405T>G
ENST00000481849.6:n.3365T>G
ENST00000497377.6:n.3272T>G
ENST00000696558.1:c.1427T>G	ENSP00000512716.1:n.1427T>G
ENST00000696559.1:c.*269T>G	ENSP00000512717.1:n.*269T>G
ENST00000696560.1:c.*269T>G	ENSP00000512718.1:n.*269T>G
ENST00000696561.1:c.*269T>G	ENSP00000512719.1:n.*269T>G
ENST00000696562.1:c.*269T>G	ENSP00000512720.1:n.*269T>G
ENST00000412585.7:c.*269T>G MANE Select	ENSP00000399168.2:n.*269T>G
ENST00000412585.6:c.*269T>G	ENSP00000399168.2:n.*269T>G
ENST00000481849.5:n.593T>G
ENST00000497377.5:n.757T>G
NM_005514.6:c.*269T>G	NP_005505.2:n.*269T>G
XM_011514556.1:c.*269T>G	XP_011512858.1:n.*269T>G
XM_011514557.1:c.*269T>G	XP_011512859.1:n.*269T>G
XR_926175.1:n.1797T>G
NM_005514.7:c.*269T>G	NP_005505.2:n.*269T>G
NM_005514.8:c.*269T>G MANE Select	NP_005505.2:n.*269T>G