Canonical Allele Identifier: CA490223166

Gene: SLC28A2-AS1

Linked Data

• dbSNP Id: rs1241502155
• MyVariant Identifiers: chr15:g.45544031A>C (hg19) ; chr15:g.45251833A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45251833A>C , CM000677.2:g.45251833A>C	GRCh38
NC_000015.9:g.45544031A>C , CM000677.1:g.45544031A>C	GRCh37
NC_000015.8:g.43331323A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120335.1:n.420T>G