Canonical Allele Identifier: CA380058927
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs2133797620

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625317G>C , CM000673.2:g.22625317G>C GRCh38
NC_000011.9:g.22646863G>C , CM000673.1:g.22646863G>C GRCh37
NC_000011.8:g.22603439G>C NCBI36
NG_007425.1:g.5525C>G , LRG_527:g.5525C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.494C>G MANE Select ENSP00000330875.3:p.Thr165Ser
ENST00000327470.4:c.494C>G ENSP00000330875.3:p.Thr165Ser
NM_022725.3:c.494C>G , LRG_527t1:c.494C>G NP_073562.1:p.Thr165Ser
NM_022725.4:c.494C>G MANE Select NP_073562.1:p.Thr165Ser