Canonical Allele Identifier: CA1222592043
Gene: HLX-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220878397G= , CM000663.2:g.220878397G= GRCh38
NC_000001.10:g.221051739G= , CM000663.1:g.221051739G= GRCh37
NC_000001.9:g.219118362G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651706.1:c.843-2797G= ENSP00000499157.1:n.843-2797G=
NR_046901.1:n.292+1452C=
XM_011510307.1:c.662C= XP_011508609.1:p.Thr221=