Canonical Allele Identifier: CA2677954694

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355004-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355005_31355006del , CM000668.2:g.31355005_31355006del	GRCh38
NC_000006.11:g.31322782_31322783del , CM000668.1:g.31322782_31322783del	GRCh37
NC_000006.10:g.31430761_31430762del	NCBI36
NG_023187.1:g.7207_7208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+101_3059+102del
ENST00000481849.6:n.2679_2680del
ENST00000497377.6:n.2586_2587del
ENST00000640094.2:c.895+311_895+312del	ENSP00000491275.2:n.895+311_895+312del
ENST00000696558.1:c.1081+101_1081+102del	ENSP00000512716.1:n.1081+101_1081+102del
ENST00000696559.1:c.1012+101_1012+102del	ENSP00000512717.1:n.1012+101_1012+102del
ENST00000696560.1:c.1012+101_1012+102del	ENSP00000512718.1:n.1012+101_1012+102del
ENST00000696561.1:c.1012+101_1012+102del	ENSP00000512719.1:n.1012+101_1012+102del
ENST00000696562.1:c.1012+101_1012+102del	ENSP00000512720.1:n.1012+101_1012+102del
ENST00000412585.7:c.1012+101_1012+102del MANE Select	ENSP00000399168.2:n.1012+101_1012+102del
ENST00000640094.1:c.88+311_88+312del	ENSP00000491275.1:n.88+311_88+312del
ENST00000412585.6:c.1012+101_1012+102del	ENSP00000399168.2:n.1012+101_1012+102del
ENST00000497377.5:n.71_72del
NM_005514.6:c.1012+101_1012+102del	NP_005505.2:n.1012+101_1012+102del
XM_011514556.1:c.1045+101_1045+102del	XP_011512858.1:n.1045+101_1045+102del
XM_011514557.1:c.895+311_895+312del	XP_011512859.1:n.895+311_895+312del
XR_926175.1:n.1451+101_1451+102del
NM_005514.7:c.1012+101_1012+102del	NP_005505.2:n.1012+101_1012+102del
NM_005514.8:c.1012+101_1012+102del MANE Select	NP_005505.2:n.1012+101_1012+102del