Canonical Allele Identifier: CA1147660518
Gene: HLX-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220837181C= , CM000663.2:g.220837181C= GRCh38
NC_000001.10:g.221010523C= , CM000663.1:g.221010523C= GRCh37
NC_000001.9:g.219077146C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31907C= ENSP00000499157.1:n.842+31907C=
NR_046901.1:n.293-3989G=