Canonical Allele Identifier: CA1619115008
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1767261541

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357627dup , CM000668.2:g.31357627dup GRCh38
NC_000006.11:g.31325404dup , CM000668.1:g.31325404dup GRCh37
NC_000006.10:g.31433383dup NCBI36
NG_023187.1:g.4586dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1325dup
ENST00000481849.6:n.1325dup
ENST00000497377.6:n.1325dup
ENST00000696559.1:c.-149dup ENSP00000512717.1:n.-149dup
ENST00000696560.1:c.-149dup ENSP00000512718.1:n.-149dup
ENST00000696561.1:c.-149dup ENSP00000512719.1:n.-149dup
ENST00000696562.1:c.-135-334dup ENSP00000512720.1:n.-135-334dup
ENST00000603274.1:n.981dup
XR_926692.1:n.151dup