Canonical Allele Identifier: CA2677958229
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357440_31357450del , CM000668.2:g.31357440_31357450del GRCh38
NC_000006.11:g.31325217_31325227del , CM000668.1:g.31325217_31325227del GRCh37
NC_000006.10:g.31433196_31433206del NCBI36
NG_023187.1:g.4763_4773del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1339-157_1339-147del
ENST00000481849.6:n.1339-157_1339-147del
ENST00000497377.6:n.1339-157_1339-147del
ENST00000696559.1:c.-135-157_-135-147del ENSP00000512717.1:n.-135-157_-135-147del
ENST00000696560.1:c.-135-157_-135-147del ENSP00000512718.1:n.-135-157_-135-147del
ENST00000696561.1:c.-135-157_-135-147del ENSP00000512719.1:n.-135-157_-135-147del
ENST00000696562.1:c.-135-157_-135-147del ENSP00000512720.1:n.-135-157_-135-147del
ENST00000603274.1:n.794_804del
XR_926692.1:n.165-157_165-147del