Canonical Allele Identifier: CA566689411

Gene: HLA-B

Linked Data

• dbSNP Id: rs1374482503
• gnomAD v2: 6-31325318-CAG-C
• gnomAD v3: 6-31357541-CAG-C
• gnomAD v4: 6-31357541-CAG-C
• MyVariant Identifiers: chr6:g.31325319_31325320del (hg19) ; chr6:g.31357542_31357543del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357542_31357543del , CM000668.2:g.31357542_31357543del	GRCh38
NC_000006.11:g.31325319_31325320del , CM000668.1:g.31325319_31325320del	GRCh37
NC_000006.10:g.31433298_31433299del	NCBI36
NG_023187.1:g.4670_4671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+71_1338+72del
ENST00000481849.6:n.1338+71_1338+72del
ENST00000497377.6:n.1338+71_1338+72del
ENST00000696559.1:c.-136+71_-136+72del	ENSP00000512717.1:n.-136+71_-136+72del
ENST00000696560.1:c.-136+71_-136+72del	ENSP00000512718.1:n.-136+71_-136+72del
ENST00000696561.1:c.-136+71_-136+72del	ENSP00000512719.1:n.-136+71_-136+72del
ENST00000696562.1:c.-135-250_-135-249del	ENSP00000512720.1:n.-135-250_-135-249del
ENST00000603274.1:n.896_897del
XR_926692.1:n.164+71_164+72del