Canonical Allele Identifier: CA2174009913
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899793354

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251671C>T , CM000677.2:g.45251671C>T GRCh38
NC_000015.9:g.45543869C>T , CM000677.1:g.45543869C>T GRCh37
NC_000015.8:g.43331161C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.582G>A