Canonical Allele Identifier: CA490222311

Gene: SLC28A2-AS1

Linked Data

• dbSNP Id: rs1260458760
• MyVariant Identifiers: chr15:g.45543902C>T (hg19) ; chr15:g.45251704C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45251704C>T , CM000677.2:g.45251704C>T	GRCh38
NC_000015.9:g.45543902C>T , CM000677.1:g.45543902C>T	GRCh37
NC_000015.8:g.43331194C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120335.1:n.549G>A