Canonical Allele Identifier: CA10975626
Gene: HLX-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs12073837

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220836863C>T , CM000663.2:g.220836863C>T GRCh38
NC_000001.10:g.221010205C>T , CM000663.1:g.221010205C>T GRCh37
NC_000001.9:g.219076828C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651706.1:c.842+31589C>T ENSP00000499157.1:n.842+31589C>T
NR_046901.1:n.293-3671G>A