Canonical Allele Identifier: CA1998596284

Gene: SLC35F2

Linked Data

• dbSNP Id: rs2186903

Genomic Alleles

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

Transcript Alleles

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