Canonical Allele Identifier: CA1012539597
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1673647152

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220837154G>T , CM000663.2:g.220837154G>T GRCh38
NC_000001.10:g.221010496G>T , CM000663.1:g.221010496G>T GRCh37
NC_000001.9:g.219077119G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31880G>T ENSP00000499157.1:n.842+31880G>T
NR_046901.1:n.293-3962C>A