Canonical Allele Identifier: CA490224200

Gene: SLC28A2-AS1

Linked Data

• gnomAD v4: 15-45251990-C-T
• MyVariant Identifiers: chr15:g.45544188C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45251990C>T , CM000677.2:g.45251990C>T	GRCh38
NC_000015.9:g.45544188C>T , CM000677.1:g.45544188C>T	GRCh37
NC_000015.8:g.43331480C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_120335.1:n.263G>A