Canonical Allele Identifier: CA2174010025
Gene: SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251777T= , CM000677.2:g.45251777T= GRCh38
NC_000015.9:g.45543975T= , CM000677.1:g.45543975T= GRCh37
NC_000015.8:g.43331267T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.476A=