Canonical Allele Identifier: CA2677954852

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355082-ACCCCACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355085_31355091del , CM000668.2:g.31355085_31355091del	GRCh38
NC_000006.11:g.31322862_31322868del , CM000668.1:g.31322862_31322868del	GRCh37
NC_000006.10:g.31430841_31430847del	NCBI36
NG_023187.1:g.7124_7130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+18_3059+24del
ENST00000481849.6:n.2596_2602del
ENST00000497377.6:n.2503_2509del
ENST00000640094.2:c.895+228_895+234del	ENSP00000491275.2:n.895+228_895+234del
ENST00000696558.1:c.1081+18_1081+24del	ENSP00000512716.1:n.1081+18_1081+24del
ENST00000696559.1:c.1012+18_1012+24del	ENSP00000512717.1:n.1012+18_1012+24del
ENST00000696560.1:c.1012+18_1012+24del	ENSP00000512718.1:n.1012+18_1012+24del
ENST00000696561.1:c.1012+18_1012+24del	ENSP00000512719.1:n.1012+18_1012+24del
ENST00000696562.1:c.1012+18_1012+24del	ENSP00000512720.1:n.1012+18_1012+24del
ENST00000412585.7:c.1012+18_1012+24del MANE Select	ENSP00000399168.2:n.1012+18_1012+24del
ENST00000640094.1:c.88+228_88+234del	ENSP00000491275.1:n.88+228_88+234del
ENST00000412585.6:c.1012+18_1012+24del	ENSP00000399168.2:n.1012+18_1012+24del
NM_005514.6:c.1012+18_1012+24del	NP_005505.2:n.1012+18_1012+24del
XM_011514556.1:c.1045+18_1045+24del	XP_011512858.1:n.1045+18_1045+24del
XM_011514557.1:c.895+228_895+234del	XP_011512859.1:n.895+228_895+234del
XR_926175.1:n.1451+18_1451+24del
NM_005514.7:c.1012+18_1012+24del	NP_005505.2:n.1012+18_1012+24del
NM_005514.8:c.1012+18_1012+24del MANE Select	NP_005505.2:n.1012+18_1012+24del