Canonical Allele Identifier: CA2677954684

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354995-C-CCCCTGGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355000_31355001insGGACCCTG , CM000668.2:g.31355000_31355001insGGACCCTG	GRCh38
NC_000006.11:g.31322777_31322778insGGACCCTG , CM000668.1:g.31322777_31322778insGGACCCTG	GRCh37
NC_000006.10:g.31430756_31430757insGGACCCTG	NCBI36
NG_023187.1:g.7217_7218insTCCCAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+111_3059+112insTCCCAGGG
ENST00000481849.6:n.2689_2690insTCCCAGGG
ENST00000497377.6:n.2596_2597insTCCCAGGG
ENST00000640094.2:c.895+321_895+322insTCCCAGGG	ENSP00000491275.2:n.895+321_895+322insTCCCAGGG
ENST00000696558.1:c.1081+111_1081+112insTCCCAGGG	ENSP00000512716.1:n.1081+111_1081+112insTCCCAGGG
ENST00000696559.1:c.1012+111_1012+112insTCCCAGGG	ENSP00000512717.1:n.1012+111_1012+112insTCCCAGGG
ENST00000696560.1:c.1012+111_1012+112insTCCCAGGG	ENSP00000512718.1:n.1012+111_1012+112insTCCCAGGG
ENST00000696561.1:c.1012+111_1012+112insTCCCAGGG	ENSP00000512719.1:n.1012+111_1012+112insTCCCAGGG
ENST00000696562.1:c.1012+111_1012+112insTCCCAGGG	ENSP00000512720.1:n.1012+111_1012+112insTCCCAGGG
ENST00000412585.7:c.1012+111_1012+112insTCCCAGGG MANE Select	ENSP00000399168.2:n.1012+111_1012+112insTCCCAGGG
ENST00000640094.1:c.88+321_88+322insTCCCAGGG	ENSP00000491275.1:n.88+321_88+322insTCCCAGGG
ENST00000412585.6:c.1012+111_1012+112insTCCCAGGG	ENSP00000399168.2:n.1012+111_1012+112insTCCCAGGG
ENST00000497377.5:n.81_82insTCCCAGGG
NM_005514.6:c.1012+111_1012+112insTCCCAGGG	NP_005505.2:n.1012+111_1012+112insTCCCAGGG
XM_011514556.1:c.1045+111_1045+112insTCCCAGGG	XP_011512858.1:n.1045+111_1045+112insTCCCAGGG
XM_011514557.1:c.895+321_895+322insTCCCAGGG	XP_011512859.1:n.895+321_895+322insTCCCAGGG
XR_926175.1:n.1451+111_1451+112insTCCCAGGG
NM_005514.7:c.1012+111_1012+112insTCCCAGGG	NP_005505.2:n.1012+111_1012+112insTCCCAGGG
NM_005514.8:c.1012+111_1012+112insTCCCAGGG MANE Select	NP_005505.2:n.1012+111_1012+112insTCCCAGGG