Canonical Allele Identifier: CA37612798
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs949764889

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836735G>A , CM000663.2:g.220836735G>A GRCh38
NC_000001.10:g.221010077G>A , CM000663.1:g.221010077G>A GRCh37
NC_000001.9:g.219076700G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31461G>A ENSP00000499157.1:n.842+31461G>A
NR_046901.1:n.293-3543C>T