Canonical Allele Identifier: CA13536155
Gene: SLC35F2 HGNC NCBI

Linked Data

dbSNP Id: rs2186903

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