Canonical Allele Identifier: CA1619114829
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs36009105

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357460dup , CM000668.2:g.31357460dup GRCh38
NC_000006.11:g.31325237dup , CM000668.1:g.31325237dup GRCh37
NC_000006.10:g.31433216dup NCBI36
NG_023187.1:g.4754dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+155dup
ENST00000481849.6:n.1338+155dup
ENST00000497377.6:n.1338+155dup
ENST00000696559.1:c.-136+155dup ENSP00000512717.1:n.-136+155dup
ENST00000696560.1:c.-136+155dup ENSP00000512718.1:n.-136+155dup
ENST00000696561.1:c.-136+155dup ENSP00000512719.1:n.-136+155dup
ENST00000696562.1:c.-135-166dup ENSP00000512720.1:n.-135-166dup
ENST00000603274.1:n.814dup
XR_926692.1:n.164+155dup