Canonical Allele Identifier: CA1957607056
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625162G= , CM000673.2:g.22625162G= GRCh38
NC_000011.9:g.22646708G= , CM000673.1:g.22646708G= GRCh37
NC_000011.8:g.22603284G= NCBI36
NG_007425.1:g.5680C= , LRG_527:g.5680C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.649C= MANE Select ENSP00000330875.3:p.Arg217=
ENST00000327470.4:c.649C= ENSP00000330875.3:p.Arg217=
NM_022725.3:c.649C= , LRG_527t1:c.649C= NP_073562.1:p.Arg217=
NM_022725.4:c.649C= MANE Select NP_073562.1:p.Arg217=