Canonical Allele Identifier: CA2677954000

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354451-C-CCCCCCCCCCTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354451_31354452insCCCCCCCCCTTA , CM000668.2:g.31354451_31354452insCCCCCCCCCTTA	GRCh38
NC_000006.11:g.31322228_31322229insCCCCCCCCCTTA , CM000668.1:g.31322228_31322229insCCCCCCCCCTTA	GRCh37
NC_000006.10:g.31430207_31430208insCCCCCCCCCTTA	NCBI36
NG_023187.1:g.7761_7762insTAAGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+27_3140+28insTAAGGGGGGGGG
ENST00000481849.6:n.3100+27_3100+28insTAAGGGGGGGGG
ENST00000497377.6:n.3007+27_3007+28insTAAGGGGGGGGG
ENST00000696558.1:c.1162+27_1162+28insTAAGGGGGGGGG	ENSP00000512716.1:n.1162+27_1162+28insTAAGGGGGGGGG
ENST00000696559.1:c.*4+27_*4+28insTAAGGGGGGGGG	ENSP00000512717.1:n.*4+27_*4+28insTAAGGGGGGGGG
ENST00000696560.1:c.*4+27_*4+28insTAAGGGGGGGGG	ENSP00000512718.1:n.*4+27_*4+28insTAAGGGGGGGGG
ENST00000696561.1:c.*4+27_*4+28insTAAGGGGGGGGG	ENSP00000512719.1:n.*4+27_*4+28insTAAGGGGGGGGG
ENST00000696562.1:c.*4+27_*4+28insTAAGGGGGGGGG	ENSP00000512720.1:n.*4+27_*4+28insTAAGGGGGGGGG
ENST00000412585.7:c.*4+27_*4+28insTAAGGGGGGGGG MANE Select	ENSP00000399168.2:n.*4+27_*4+28insTAAGGGGGGGGG
ENST00000412585.6:c.*4+27_*4+28insTAAGGGGGGGGG	ENSP00000399168.2:n.*4+27_*4+28insTAAGGGGGGGGG
ENST00000481849.5:n.328+27_328+28insTAAGGGGGGGGG
ENST00000497377.5:n.492+27_492+28insTAAGGGGGGGGG
NM_005514.6:c.*4+27_*4+28insTAAGGGGGGGGG	NP_005505.2:n.*4+27_*4+28insTAAGGGGGGGGG
XM_011514556.1:c.*4+27_*4+28insTAAGGGGGGGGG	XP_011512858.1:n.*4+27_*4+28insTAAGGGGGGGGG
XM_011514557.1:c.*4+27_*4+28insTAAGGGGGGGGG	XP_011512859.1:n.*4+27_*4+28insTAAGGGGGGGGG
XR_926175.1:n.1532+27_1532+28insTAAGGGGGGGGG
NM_005514.7:c.*4+27_*4+28insTAAGGGGGGGGG	NP_005505.2:n.*4+27_*4+28insTAAGGGGGGGGG
NM_005514.8:c.*4+27_*4+28insTAAGGGGGGGGG MANE Select	NP_005505.2:n.*4+27_*4+28insTAAGGGGGGGGG