Canonical Allele Identifier: CA490222246
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45543890G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251692G>T , CM000677.2:g.45251692G>T GRCh38
NC_000015.9:g.45543890G>T , CM000677.1:g.45543890G>T GRCh37
NC_000015.8:g.43331182G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.561C>A