Canonical Allele Identifier: CA1957607145
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625332T= , CM000673.2:g.22625332T= GRCh38
NC_000011.9:g.22646878T= , CM000673.1:g.22646878T= GRCh37
NC_000011.8:g.22603454T= NCBI36
NG_007425.1:g.5510A= , LRG_527:g.5510A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.479A= MANE Select ENSP00000330875.3:p.Asp160=
ENST00000327470.4:c.479A= ENSP00000330875.3:p.Asp160=
NM_022725.3:c.479A= , LRG_527t1:c.479A= NP_073562.1:p.Asp160=
NM_022725.4:c.479A= MANE Select NP_073562.1:p.Asp160=