Canonical Allele Identifier: CA1619114993
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357623T= , CM000668.2:g.31357623T= GRCh38
NC_000006.11:g.31325400T= , CM000668.1:g.31325400T= GRCh37
NC_000006.10:g.31433379T= NCBI36
NG_023187.1:g.4590A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1329A=
ENST00000481849.6:n.1329A=
ENST00000497377.6:n.1329A=
ENST00000696559.1:c.-145A= ENSP00000512717.1:n.-145A=
ENST00000696560.1:c.-145A= ENSP00000512718.1:n.-145A=
ENST00000696561.1:c.-145A= ENSP00000512719.1:n.-145A=
ENST00000696562.1:c.-135-330A= ENSP00000512720.1:n.-135-330A=
ENST00000603274.1:n.977T=
XR_926692.1:n.155A=