Canonical Allele Identifier: CA15634182

Gene: SLC29A3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71376162G>A , CM000672.2:g.71376162G>A	GRCh38
NC_000010.10:g.73135919G>A , CM000672.1:g.73135919G>A	GRCh37
NC_000010.9:g.72805925G>A	NCBI36
NG_017066.2:g.61904G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642772.1:c.*211+351G>A	ENSP00000495041.1:n.*211+351G>A
ENST00000644895.1:c.*216+351G>A	ENSP00000493872.1:n.*216+351G>A