Canonical Allele Identifier: CA136836845

Gene: HLA-B

Linked Data

• dbSNP Id: rs67366970
• gnomAD v2: 6-31325338-CTCG-C
• gnomAD v3: 6-31357561-CTCG-C
• gnomAD v4: 6-31357561-CTCG-C
• MyVariant Identifiers: chr6:g.31325339_31325341del (hg19) ; chr6:g.31357562_31357564del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357564_31357566del , CM000668.2:g.31357564_31357566del	GRCh38
NC_000006.11:g.31325341_31325343del , CM000668.1:g.31325341_31325343del	GRCh37
NC_000006.10:g.31433320_31433322del	NCBI36
NG_023187.1:g.4649_4651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+50_1338+52del
ENST00000481849.6:n.1338+50_1338+52del
ENST00000497377.6:n.1338+50_1338+52del
ENST00000696559.1:c.-136+50_-136+52del	ENSP00000512717.1:n.-136+50_-136+52del
ENST00000696560.1:c.-136+50_-136+52del	ENSP00000512718.1:n.-136+50_-136+52del
ENST00000696561.1:c.-136+50_-136+52del	ENSP00000512719.1:n.-136+50_-136+52del
ENST00000696562.1:c.-135-271_-135-269del	ENSP00000512720.1:n.-135-271_-135-269del
ENST00000603274.1:n.918_920del
XR_926692.1:n.164+50_164+52del