Canonical Allele Identifier: CA1619117957

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766782137

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355004_31355005insGATGCTGCT , CM000668.2:g.31355004_31355005insGATGCTGCT	GRCh38
NC_000006.11:g.31322781_31322782insGATGCTGCT , CM000668.1:g.31322781_31322782insGATGCTGCT	GRCh37
NC_000006.10:g.31430760_31430761insGATGCTGCT	NCBI36
NG_023187.1:g.7208_7209insAGCAGCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+102_3059+103insAGCAGCATC
ENST00000481849.6:n.2680_2681insAGCAGCATC
ENST00000497377.6:n.2587_2588insAGCAGCATC
ENST00000640094.2:c.895+312_895+313insAGCAGCATC	ENSP00000491275.2:n.895+312_895+313insAGCAGCATC
ENST00000696558.1:c.1081+102_1081+103insAGCAGCATC	ENSP00000512716.1:n.1081+102_1081+103insAGCAGCATC
ENST00000696559.1:c.1012+102_1012+103insAGCAGCATC	ENSP00000512717.1:n.1012+102_1012+103insAGCAGCATC
ENST00000696560.1:c.1012+102_1012+103insAGCAGCATC	ENSP00000512718.1:n.1012+102_1012+103insAGCAGCATC
ENST00000696561.1:c.1012+102_1012+103insAGCAGCATC	ENSP00000512719.1:n.1012+102_1012+103insAGCAGCATC
ENST00000696562.1:c.1012+102_1012+103insAGCAGCATC	ENSP00000512720.1:n.1012+102_1012+103insAGCAGCATC
ENST00000412585.7:c.1012+102_1012+103insAGCAGCATC MANE Select	ENSP00000399168.2:n.1012+102_1012+103insAGCAGCATC
ENST00000640094.1:c.88+312_88+313insAGCAGCATC	ENSP00000491275.1:n.88+312_88+313insAGCAGCATC
ENST00000412585.6:c.1012+102_1012+103insAGCAGCATC	ENSP00000399168.2:n.1012+102_1012+103insAGCAGCATC
ENST00000497377.5:n.72_73insAGCAGCATC
NM_005514.6:c.1012+102_1012+103insAGCAGCATC	NP_005505.2:n.1012+102_1012+103insAGCAGCATC
XM_011514556.1:c.1045+102_1045+103insAGCAGCATC	XP_011512858.1:n.1045+102_1045+103insAGCAGCATC
XM_011514557.1:c.895+312_895+313insAGCAGCATC	XP_011512859.1:n.895+312_895+313insAGCAGCATC
XR_926175.1:n.1451+102_1451+103insAGCAGCATC
NM_005514.7:c.1012+102_1012+103insAGCAGCATC	NP_005505.2:n.1012+102_1012+103insAGCAGCATC
NM_005514.8:c.1012+102_1012+103insAGCAGCATC MANE Select	NP_005505.2:n.1012+102_1012+103insAGCAGCATC