Canonical Allele Identifier: CA270151049

Gene: SLC28A2-AS1

Linked Data

• dbSNP Id: rs769738345
• gnomAD v4: 15-45251928-A-T
• MyVariant Identifiers: chr15:g.45544126A>T (hg19) ; chr15:g.45251928A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45251928A>T , CM000677.2:g.45251928A>T	GRCh38
NC_000015.9:g.45544126A>T , CM000677.1:g.45544126A>T	GRCh37
NC_000015.8:g.43331418A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120335.1:n.325T>A