Canonical Allele Identifier: CA13536155

Gene: SLC35F2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.107885825G>A , CM000673.2:g.107885825G>A	GRCh38
NC_000011.9:g.107756551G>A , CM000673.1:g.107756551G>A	GRCh37
NC_000011.8:g.107261761G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525071.5:c.-349+22616C>T	ENSP00000434307.1:n.-349+22616C>T