Canonical Allele Identifier: CA1222592080
Gene: HLX-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220878474T= , CM000663.2:g.220878474T= GRCh38
NC_000001.10:g.221051816T= , CM000663.1:g.221051816T= GRCh37
NC_000001.9:g.219118439T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.843-2720T= ENSP00000499157.1:n.843-2720T=
NR_046901.1:n.292+1375A=
XM_011510307.1:c.585A= XP_011508609.1:p.Pro195=