Canonical Allele Identifier: CA2677958290

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357539-C-CTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357539_31357540insTCA , CM000668.2:g.31357539_31357540insTCA	GRCh38
NC_000006.11:g.31325316_31325317insTCA , CM000668.1:g.31325316_31325317insTCA	GRCh37
NC_000006.10:g.31433295_31433296insTCA	NCBI36
NG_023187.1:g.4673_4674insTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+74_1338+75insTGA
ENST00000481849.6:n.1338+74_1338+75insTGA
ENST00000497377.6:n.1338+74_1338+75insTGA
ENST00000696559.1:c.-136+74_-136+75insTGA	ENSP00000512717.1:n.-136+74_-136+75insTGA
ENST00000696560.1:c.-136+74_-136+75insTGA	ENSP00000512718.1:n.-136+74_-136+75insTGA
ENST00000696561.1:c.-136+74_-136+75insTGA	ENSP00000512719.1:n.-136+74_-136+75insTGA
ENST00000696562.1:c.-135-247_-135-246insTGA	ENSP00000512720.1:n.-135-247_-135-246insTGA
ENST00000603274.1:n.893_894insTCA
XR_926692.1:n.164+74_164+75insTGA