Canonical Allele Identifier: CA2770503568

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355152_31355157del , CM000668.2:g.31355152_31355157del	GRCh38
NC_000006.11:g.31322929_31322934del , CM000668.1:g.31322929_31322934del	GRCh37
NC_000006.10:g.31430908_31430913del	NCBI36
NG_023187.1:g.7057_7062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3010_3015del
ENST00000481849.6:n.2529_2534del
ENST00000497377.6:n.2436_2441del
ENST00000640094.2:c.895+161_895+166del	ENSP00000491275.2:n.895+161_895+166del
ENST00000696558.1:c.1032_1037del	ENSP00000512716.1:n.1032_1037del
ENST00000696559.1:c.963_968del	ENSP00000512717.1:p.Val322_Ile323del
ENST00000696560.1:c.963_968del	ENSP00000512718.1:p.Val322_Ile323del
ENST00000696561.1:c.963_968del	ENSP00000512719.1:p.Val322_Ile323del
ENST00000696562.1:c.963_968del	ENSP00000512720.1:p.Val322_Ile323del
ENST00000412585.7:c.963_968del MANE Select	ENSP00000399168.2:p.Val322_Ile323del
ENST00000640094.1:c.88+161_88+166del	ENSP00000491275.1:n.88+161_88+166del
ENST00000412585.6:c.963_968del	ENSP00000399168.2:p.Val322_Ile323del
ENST00000463574.1:n.554_559del
NM_005514.6:c.963_968del	NP_005505.2:p.Val322_Ile323del
XM_011514556.1:c.996_1001del	XP_011512858.1:p.Val333_Ile334del
XM_011514557.1:c.895+161_895+166del	XP_011512859.1:n.895+161_895+166del
XR_926175.1:n.1402_1407del
NM_005514.7:c.963_968del	NP_005505.2:p.Val322_Ile323del
NM_005514.8:c.963_968del MANE Select	NP_005505.2:p.Val322_Ile323del