Canonical Allele Identifier: CA1619114693
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1767223330

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357349del , CM000668.2:g.31357349del GRCh38
NC_000006.11:g.31325126del , CM000668.1:g.31325126del GRCh37
NC_000006.10:g.31433105del NCBI36
NG_023187.1:g.4867del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-53del
ENST00000481849.6:n.1339-53del
ENST00000497377.6:n.1339-53del
ENST00000696559.1:c.-135-53del ENSP00000512717.1:n.-135-53del
ENST00000696560.1:c.-135-53del ENSP00000512718.1:n.-135-53del
ENST00000696561.1:c.-135-53del ENSP00000512719.1:n.-135-53del
ENST00000696562.1:c.-135-53del ENSP00000512720.1:n.-135-53del
ENST00000603274.1:n.703del
XR_926692.1:n.165-53del