Canonical Allele Identifier: CA490224218
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899803317
MyVariant Identifiers: chr15:g.45544191T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251993T>G , CM000677.2:g.45251993T>G GRCh38
NC_000015.9:g.45544191T>G , CM000677.1:g.45544191T>G GRCh37
NC_000015.8:g.43331483T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120335.1:n.260A>C