Canonical Allele Identifier: CA270151076
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs897021119

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251939G>A , CM000677.2:g.45251939G>A GRCh38
NC_000015.9:g.45544137G>A , CM000677.1:g.45544137G>A GRCh37
NC_000015.8:g.43331429G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.314C>T