Canonical Allele Identifier: CA490222806

Gene: SLC28A2-AS1

Linked Data

• gnomAD v4: 15-45251786-G-T
• MyVariant Identifiers: chr15:g.45543984G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45251786G>T , CM000677.2:g.45251786G>T	GRCh38
NC_000015.9:g.45543984G>T , CM000677.1:g.45543984G>T	GRCh37
NC_000015.8:g.43331276G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120335.1:n.467C>A