Canonical Allele Identifier: CA490224210
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45544190A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251992A>C , CM000677.2:g.45251992A>C GRCh38
NC_000015.9:g.45544190A>C , CM000677.1:g.45544190A>C GRCh37
NC_000015.8:g.43331482A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120335.1:n.261T>G