Canonical Allele Identifier: CA380059208
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625453C>T , CM000673.2:g.22625453C>T GRCh38
NC_000011.9:g.22646999C>T , CM000673.1:g.22646999C>T GRCh37
NC_000011.8:g.22603575C>T NCBI36
NG_007425.1:g.5389G>A , LRG_527:g.5389G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.358G>A MANE Select ENSP00000330875.3:p.Gly120Ser
ENST00000327470.4:c.358G>A ENSP00000330875.3:p.Gly120Ser
NM_022725.3:c.358G>A , LRG_527t1:c.358G>A NP_073562.1:p.Gly120Ser
NM_022725.4:c.358G>A MANE Select NP_073562.1:p.Gly120Ser