Canonical Allele Identifier: CA37612793
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs189533604

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836733T>C , CM000663.2:g.220836733T>C GRCh38
NC_000001.10:g.221010075T>C , CM000663.1:g.221010075T>C GRCh37
NC_000001.9:g.219076698T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31459T>C ENSP00000499157.1:n.842+31459T>C
NR_046901.1:n.293-3541A>G