Canonical Allele Identifier: CA490222682
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45543963T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251765T>G , CM000677.2:g.45251765T>G GRCh38
NC_000015.9:g.45543963T>G , CM000677.1:g.45543963T>G GRCh37
NC_000015.8:g.43331255T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.488A>C
Search 100 bp 5'
Search 100 bp 3'