Canonical Allele Identifier: CA270150892
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs959502392

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251758A>G , CM000677.2:g.45251758A>G GRCh38
NC_000015.9:g.45543956A>G , CM000677.1:g.45543956A>G GRCh37
NC_000015.8:g.43331248A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.495T>C