Canonical Allele Identifier: CA1957607046
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625147A= , CM000673.2:g.22625147A= GRCh38
NC_000011.9:g.22646693A= , CM000673.1:g.22646693A= GRCh37
NC_000011.8:g.22603269A= NCBI36
NG_007425.1:g.5695T= , LRG_527:g.5695T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.664T= MANE Select ENSP00000330875.3:p.Leu222=
ENST00000327470.4:c.664T= ENSP00000330875.3:p.Leu222=
NM_022725.3:c.664T= , LRG_527t1:c.664T= NP_073562.1:p.Leu222=
NM_022725.4:c.664T= MANE Select NP_073562.1:p.Leu222=