Canonical Allele Identifier: CA2174009995
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251757C= , CM000677.2:g.45251757C= GRCh38
NC_000015.9:g.45543955C= , CM000677.1:g.45543955C= GRCh37
NC_000015.8:g.43331247C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.496G=