Canonical Allele Identifier: CA380058508
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs2133797029

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625111T>C , CM000673.2:g.22625111T>C GRCh38
NC_000011.9:g.22646657T>C , CM000673.1:g.22646657T>C GRCh37
NC_000011.8:g.22603233T>C NCBI36
NG_007425.1:g.5731A>G , LRG_527:g.5731A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.700A>G MANE Select ENSP00000330875.3:p.Ser234Gly
ENST00000327470.4:c.700A>G ENSP00000330875.3:p.Ser234Gly
NM_022725.3:c.700A>G , LRG_527t1:c.700A>G NP_073562.1:p.Ser234Gly
NM_022725.4:c.700A>G MANE Select NP_073562.1:p.Ser234Gly