Canonical Allele Identifier: CA2677958308
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357579_31357598del , CM000668.2:g.31357579_31357598del GRCh38
NC_000006.11:g.31325356_31325375del , CM000668.1:g.31325356_31325375del GRCh37
NC_000006.10:g.31433335_31433354del NCBI36
NG_023187.1:g.4621_4640del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+22_1338+41del
ENST00000481849.6:n.1338+22_1338+41del
ENST00000497377.6:n.1338+22_1338+41del
ENST00000696559.1:c.-136+22_-136+41del ENSP00000512717.1:n.-136+22_-136+41del
ENST00000696560.1:c.-136+22_-136+41del ENSP00000512718.1:n.-136+22_-136+41del
ENST00000696561.1:c.-136+22_-136+41del ENSP00000512719.1:n.-136+22_-136+41del
ENST00000696562.1:c.-135-299_-135-280del ENSP00000512720.1:n.-135-299_-135-280del
ENST00000603274.1:n.933_952del
XR_926692.1:n.164+22_164+41del