Canonical Allele Identifier: CA2677954685

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354998-C-CATAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354998_31354999insATAAT , CM000668.2:g.31354998_31354999insATAAT	GRCh38
NC_000006.11:g.31322775_31322776insATAAT , CM000668.1:g.31322775_31322776insATAAT	GRCh37
NC_000006.10:g.31430754_31430755insATAAT	NCBI36
NG_023187.1:g.7214_7215insATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+108_3059+109insATTAT
ENST00000481849.6:n.2686_2687insATTAT
ENST00000497377.6:n.2593_2594insATTAT
ENST00000640094.2:c.895+318_895+319insATTAT	ENSP00000491275.2:n.895+318_895+319insATTAT
ENST00000696558.1:c.1081+108_1081+109insATTAT	ENSP00000512716.1:n.1081+108_1081+109insATTAT
ENST00000696559.1:c.1012+108_1012+109insATTAT	ENSP00000512717.1:n.1012+108_1012+109insATTAT
ENST00000696560.1:c.1012+108_1012+109insATTAT	ENSP00000512718.1:n.1012+108_1012+109insATTAT
ENST00000696561.1:c.1012+108_1012+109insATTAT	ENSP00000512719.1:n.1012+108_1012+109insATTAT
ENST00000696562.1:c.1012+108_1012+109insATTAT	ENSP00000512720.1:n.1012+108_1012+109insATTAT
ENST00000412585.7:c.1012+108_1012+109insATTAT MANE Select	ENSP00000399168.2:n.1012+108_1012+109insATTAT
ENST00000640094.1:c.88+318_88+319insATTAT	ENSP00000491275.1:n.88+318_88+319insATTAT
ENST00000412585.6:c.1012+108_1012+109insATTAT	ENSP00000399168.2:n.1012+108_1012+109insATTAT
ENST00000497377.5:n.78_79insATTAT
NM_005514.6:c.1012+108_1012+109insATTAT	NP_005505.2:n.1012+108_1012+109insATTAT
XM_011514556.1:c.1045+108_1045+109insATTAT	XP_011512858.1:n.1045+108_1045+109insATTAT
XM_011514557.1:c.895+318_895+319insATTAT	XP_011512859.1:n.895+318_895+319insATTAT
XR_926175.1:n.1451+108_1451+109insATTAT
NM_005514.7:c.1012+108_1012+109insATTAT	NP_005505.2:n.1012+108_1012+109insATTAT
NM_005514.8:c.1012+108_1012+109insATTAT MANE Select	NP_005505.2:n.1012+108_1012+109insATTAT