Canonical Allele Identifier: CA490224252

Gene: SLC28A2-AS1

Linked Data

• gnomAD v4: 15-45251999-C-A
• MyVariant Identifiers: chr15:g.45544197C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45251999C>A , CM000677.2:g.45251999C>A	GRCh38
NC_000015.9:g.45544197C>A , CM000677.1:g.45544197C>A	GRCh37
NC_000015.8:g.43331489C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120335.1:n.254G>T