Canonical Allele Identifier: CA37612762
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs113995875

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836660A>G , CM000663.2:g.220836660A>G GRCh38
NC_000001.10:g.221010002A>G , CM000663.1:g.221010002A>G GRCh37
NC_000001.9:g.219076625A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+31386A>G ENSP00000499157.1:n.842+31386A>G
NR_046901.1:n.293-3468T>C