Canonical Allele Identifier: CA2174010005
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251759G= , CM000677.2:g.45251759G= GRCh38
NC_000015.9:g.45543957G= , CM000677.1:g.45543957G= GRCh37
NC_000015.8:g.43331249G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.494C=