Canonical Allele Identifier: CA490222560
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1337301389
MyVariant Identifiers: chr15:g.45543945G>C (hg19) chr15:g.45251747G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251747G>C , CM000677.2:g.45251747G>C GRCh38
NC_000015.9:g.45543945G>C , CM000677.1:g.45543945G>C GRCh37
NC_000015.8:g.43331237G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.506C>G
Search 100 bp 5'
Search 100 bp 3'