Canonical Allele Identifier: CA1222592051
Gene: HLX-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220878423A= , CM000663.2:g.220878423A= GRCh38
NC_000001.10:g.221051765A= , CM000663.1:g.221051765A= GRCh37
NC_000001.9:g.219118388A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.843-2771A= ENSP00000499157.1:n.843-2771A=
NR_046901.1:n.292+1426T=
XM_011510307.1:c.636T= XP_011508609.1:p.Leu212=