Canonical Allele Identifier: CA2677953101

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354142-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354142_31354143insGA , CM000668.2:g.31354142_31354143insGA	GRCh38
NC_000006.11:g.31321919_31321920insGA , CM000668.1:g.31321919_31321920insGA	GRCh37
NC_000006.10:g.31429898_31429899insGA	NCBI36
NG_023187.1:g.8070_8071insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3294_3295insTC
ENST00000481849.6:n.3254_3255insTC
ENST00000497377.6:n.3161_3162insTC
ENST00000696558.1:c.1316_1317insTC	ENSP00000512716.1:n.1316_1317insTC
ENST00000696559.1:c.*158_*159insTC	ENSP00000512717.1:n.*158_*159insTC
ENST00000696560.1:c.*158_*159insTC	ENSP00000512718.1:n.*158_*159insTC
ENST00000696561.1:c.*158_*159insTC	ENSP00000512719.1:n.*158_*159insTC
ENST00000696562.1:c.*158_*159insTC	ENSP00000512720.1:n.*158_*159insTC
ENST00000412585.7:c.*158_*159insTC MANE Select	ENSP00000399168.2:n.*158_*159insTC
ENST00000412585.6:c.*158_*159insTC	ENSP00000399168.2:n.*158_*159insTC
ENST00000481849.5:n.482_483insTC
ENST00000497377.5:n.646_647insTC
NM_005514.6:c.*158_*159insTC	NP_005505.2:n.*158_*159insTC
XM_011514556.1:c.*158_*159insTC	XP_011512858.1:n.*158_*159insTC
XM_011514557.1:c.*158_*159insTC	XP_011512859.1:n.*158_*159insTC
XR_926175.1:n.1686_1687insTC
NM_005514.7:c.*158_*159insTC	NP_005505.2:n.*158_*159insTC
NM_005514.8:c.*158_*159insTC MANE Select	NP_005505.2:n.*158_*159insTC