Canonical Allele Identifier: CA2730596903
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1247776293

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251680C>T , CM000677.2:g.45251680C>T GRCh38
NC_000015.9:g.45543878C>T , CM000677.1:g.45543878C>T GRCh37
NC_000015.8:g.43331170C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.573G>A