Canonical Allele Identifier: CA2174010011
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251763T= , CM000677.2:g.45251763T= GRCh38
NC_000015.9:g.45543961T= , CM000677.1:g.45543961T= GRCh37
NC_000015.8:g.43331253T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.490A=