Canonical Allele Identifier: CA1957607148
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625337C= , CM000673.2:g.22625337C= GRCh38
NC_000011.9:g.22646883C= , CM000673.1:g.22646883C= GRCh37
NC_000011.8:g.22603459C= NCBI36
NG_007425.1:g.5505G= , LRG_527:g.5505G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.474G= MANE Select ENSP00000330875.3:p.Gln158=
ENST00000327470.4:c.474G= ENSP00000330875.3:p.Gln158=
NM_022725.3:c.474G= , LRG_527t1:c.474G= NP_073562.1:p.Gln158=
NM_022725.4:c.474G= MANE Select NP_073562.1:p.Gln158=