Canonical Allele Identifier: CA2677955042

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355153-GACC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355156_31355158del , CM000668.2:g.31355156_31355158del	GRCh38
NC_000006.11:g.31322933_31322935del , CM000668.1:g.31322933_31322935del	GRCh37
NC_000006.10:g.31430912_31430914del	NCBI36
NG_023187.1:g.7057_7059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3010_3012del
ENST00000481849.6:n.2529_2531del
ENST00000497377.6:n.2436_2438del
ENST00000640094.2:c.895+161_895+163del	ENSP00000491275.2:n.895+161_895+163del
ENST00000696558.1:c.1032_1034del	ENSP00000512716.1:n.1032_1034del
ENST00000696559.1:c.963_965del	ENSP00000512717.1:p.Val322del
ENST00000696560.1:c.963_965del	ENSP00000512718.1:p.Val322del
ENST00000696561.1:c.963_965del	ENSP00000512719.1:p.Val322del
ENST00000696562.1:c.963_965del	ENSP00000512720.1:p.Val322del
ENST00000412585.7:c.963_965del MANE Select	ENSP00000399168.2:p.Val322del
ENST00000640094.1:c.88+161_88+163del	ENSP00000491275.1:n.88+161_88+163del
ENST00000412585.6:c.963_965del	ENSP00000399168.2:p.Val322del
ENST00000463574.1:n.554_556del
NM_005514.6:c.963_965del	NP_005505.2:p.Val322del
XM_011514556.1:c.996_998del	XP_011512858.1:p.Val333del
XM_011514557.1:c.895+161_895+163del	XP_011512859.1:n.895+161_895+163del
XR_926175.1:n.1402_1404del
NM_005514.7:c.963_965del	NP_005505.2:p.Val322del
NM_005514.8:c.963_965del MANE Select	NP_005505.2:p.Val322del