Canonical Allele Identifier: CA490222301
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45543900T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251702T>C , CM000677.2:g.45251702T>C GRCh38
NC_000015.9:g.45543900T>C , CM000677.1:g.45543900T>C GRCh37
NC_000015.8:g.43331192T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.551A>G