Canonical Allele Identifier: CA490222725
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45543969T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251771T>G , CM000677.2:g.45251771T>G GRCh38
NC_000015.9:g.45543969T>G , CM000677.1:g.45543969T>G GRCh37
NC_000015.8:g.43331261T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.482A>C