Canonical Allele Identifier: CA731823942
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1312610362

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836627A>T , CM000663.2:g.220836627A>T GRCh38
NC_000001.10:g.221009969A>T , CM000663.1:g.221009969A>T GRCh37
NC_000001.9:g.219076592A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31353A>T ENSP00000499157.1:n.842+31353A>T
NR_046901.1:n.293-3435T>A