Canonical Allele Identifier: CA2174010097
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251839C= , CM000677.2:g.45251839C= GRCh38
NC_000015.9:g.45544037C= , CM000677.1:g.45544037C= GRCh37
NC_000015.8:g.43331329C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.414G=