Canonical Allele Identifier: CA529064257
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1391042409

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836839C>A , CM000663.2:g.220836839C>A GRCh38
NC_000001.10:g.221010181C>A , CM000663.1:g.221010181C>A GRCh37
NC_000001.9:g.219076804C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31565C>A ENSP00000499157.1:n.842+31565C>A
NR_046901.1:n.293-3647G>T