Canonical Allele Identifier: CA1222592092
Gene: HLX-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220878499G= , CM000663.2:g.220878499G= GRCh38
NC_000001.10:g.221051841G= , CM000663.1:g.221051841G= GRCh37
NC_000001.9:g.219118464G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.843-2695G= ENSP00000499157.1:n.843-2695G=
NR_046901.1:n.292+1350C=
XM_011510307.1:c.560C= XP_011508609.1:p.Ala187=