Canonical Allele Identifier: CA1087463988

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355021-A-ATC
• gnomAD v4: 6-31355021-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355021_31355022insTC , CM000668.2:g.31355021_31355022insTC	GRCh38
NC_000006.11:g.31322798_31322799insTC , CM000668.1:g.31322798_31322799insTC	GRCh37
NC_000006.10:g.31430777_31430778insTC	NCBI36
NG_023187.1:g.7191_7192insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+85_3059+86insGA
ENST00000481849.6:n.2663_2664insGA
ENST00000497377.6:n.2570_2571insGA
ENST00000640094.2:c.895+295_895+296insGA	ENSP00000491275.2:n.895+295_895+296insGA
ENST00000696558.1:c.1081+85_1081+86insGA	ENSP00000512716.1:n.1081+85_1081+86insGA
ENST00000696559.1:c.1012+85_1012+86insGA	ENSP00000512717.1:n.1012+85_1012+86insGA
ENST00000696560.1:c.1012+85_1012+86insGA	ENSP00000512718.1:n.1012+85_1012+86insGA
ENST00000696561.1:c.1012+85_1012+86insGA	ENSP00000512719.1:n.1012+85_1012+86insGA
ENST00000696562.1:c.1012+85_1012+86insGA	ENSP00000512720.1:n.1012+85_1012+86insGA
ENST00000412585.7:c.1012+85_1012+86insGA MANE Select	ENSP00000399168.2:n.1012+85_1012+86insGA
ENST00000640094.1:c.88+295_88+296insGA	ENSP00000491275.1:n.88+295_88+296insGA
ENST00000412585.6:c.1012+85_1012+86insGA	ENSP00000399168.2:n.1012+85_1012+86insGA
ENST00000497377.5:n.55_56insGA
NM_005514.6:c.1012+85_1012+86insGA	NP_005505.2:n.1012+85_1012+86insGA
XM_011514556.1:c.1045+85_1045+86insGA	XP_011512858.1:n.1045+85_1045+86insGA
XM_011514557.1:c.895+295_895+296insGA	XP_011512859.1:n.895+295_895+296insGA
XR_926175.1:n.1451+85_1451+86insGA
NM_005514.7:c.1012+85_1012+86insGA	NP_005505.2:n.1012+85_1012+86insGA
NM_005514.8:c.1012+85_1012+86insGA MANE Select	NP_005505.2:n.1012+85_1012+86insGA