Canonical Allele Identifier: CA1957607058
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625167G= , CM000673.2:g.22625167G= GRCh38
NC_000011.9:g.22646713G= , CM000673.1:g.22646713G= GRCh37
NC_000011.8:g.22603289G= NCBI36
NG_007425.1:g.5675C= , LRG_527:g.5675C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.644C= MANE Select ENSP00000330875.3:p.Ser215=
ENST00000327470.4:c.644C= ENSP00000330875.3:p.Ser215=
NM_022725.3:c.644C= , LRG_527t1:c.644C= NP_073562.1:p.Ser215=
NM_022725.4:c.644C= MANE Select NP_073562.1:p.Ser215=