Canonical Allele Identifier: CA2174009918
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899793608

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251673G>C , CM000677.2:g.45251673G>C GRCh38
NC_000015.9:g.45543871G>C , CM000677.1:g.45543871G>C GRCh37
NC_000015.8:g.43331163G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.580C>G