Canonical Allele Identifier: CA490223112
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45544024C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251826C>A , CM000677.2:g.45251826C>A GRCh38
NC_000015.9:g.45544024C>A , CM000677.1:g.45544024C>A GRCh37
NC_000015.8:g.43331316C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.427G>T