Canonical Allele Identifier: CA1222592028
Gene: HLX-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220878366T= , CM000663.2:g.220878366T= GRCh38
NC_000001.10:g.221051708T= , CM000663.1:g.221051708T= GRCh37
NC_000001.9:g.219118331T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.843-2828T= ENSP00000499157.1:n.843-2828T=
NR_046901.1:n.292+1483A=
XM_011510307.1:c.687+6A= XP_011508609.1:n.687+6A=