Canonical Allele Identifier: CA490224206
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899803256
MyVariant Identifiers: chr15:g.45544189G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251991G>C , CM000677.2:g.45251991G>C GRCh38
NC_000015.9:g.45544189G>C , CM000677.1:g.45544189G>C GRCh37
NC_000015.8:g.43331481G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120335.1:n.262C>G