Canonical Allele Identifier: CA1957607002
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625071A= , CM000673.2:g.22625071A= GRCh38
NC_000011.9:g.22646617A= , CM000673.1:g.22646617A= GRCh37
NC_000011.8:g.22603193A= NCBI36
NG_007425.1:g.5771T= , LRG_527:g.5771T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.740T= MANE Select ENSP00000330875.3:p.Val247=
ENST00000327470.4:c.740T= ENSP00000330875.3:p.Val247=
NM_022725.3:c.740T= , LRG_527t1:c.740T= NP_073562.1:p.Val247=
NM_022725.4:c.740T= MANE Select NP_073562.1:p.Val247=