Canonical Allele Identifier: CA1619114999
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1767261188

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357626del , CM000668.2:g.31357626del GRCh38
NC_000006.11:g.31325403del , CM000668.1:g.31325403del GRCh37
NC_000006.10:g.31433382del NCBI36
NG_023187.1:g.4587del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1326del
ENST00000481849.6:n.1326del
ENST00000497377.6:n.1326del
ENST00000696559.1:c.-148del ENSP00000512717.1:n.-148del
ENST00000696560.1:c.-148del ENSP00000512718.1:n.-148del
ENST00000696561.1:c.-148del ENSP00000512719.1:n.-148del
ENST00000696562.1:c.-135-333del ENSP00000512720.1:n.-135-333del
ENST00000603274.1:n.980del
XR_926692.1:n.152del