Canonical Allele Identifier: CA2174010008
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251760A= , CM000677.2:g.45251760A= GRCh38
NC_000015.9:g.45543958A= , CM000677.1:g.45543958A= GRCh37
NC_000015.8:g.43331250A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.493T=