Canonical Allele Identifier: CA490224185

Gene: SLC28A2-AS1

Linked Data

• dbSNP Id: rs1899803168
• gnomAD v4: 15-45251988-A-G
• MyVariant Identifiers: chr15:g.45544186A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45251988A>G , CM000677.2:g.45251988A>G	GRCh38
NC_000015.9:g.45544186A>G , CM000677.1:g.45544186A>G	GRCh37
NC_000015.8:g.43331478A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120335.1:n.265T>C