Canonical Allele Identifier: CA2698210607
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2102624749

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220837279A>C , CM000663.2:g.220837279A>C GRCh38
NC_000001.10:g.221010621A>C , CM000663.1:g.221010621A>C GRCh37
NC_000001.9:g.219077244A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651706.1:c.842+32005A>C ENSP00000499157.1:n.842+32005A>C
NR_046901.1:n.293-4087T>G