Canonical Allele Identifier: CA490223098
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1899796961
MyVariant Identifiers: chr15:g.45544021T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251823T>G , CM000677.2:g.45251823T>G GRCh38
NC_000015.9:g.45544021T>G , CM000677.1:g.45544021T>G GRCh37
NC_000015.8:g.43331313T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.430A>C