Canonical Allele Identifier: CA2174009940
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251689A= , CM000677.2:g.45251689A= GRCh38
NC_000015.9:g.45543887A= , CM000677.1:g.45543887A= GRCh37
NC_000015.8:g.43331179A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.564T=