Canonical Allele Identifier: CA1957606932
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624943G= , CM000673.2:g.22624943G= GRCh38
NC_000011.9:g.22646489G= , CM000673.1:g.22646489G= GRCh37
NC_000011.8:g.22603065G= NCBI36
NG_007425.1:g.5899C= , LRG_527:g.5899C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.868C= MANE Select ENSP00000330875.3:p.Gln290=
ENST00000327470.4:c.868C= ENSP00000330875.3:p.Gln290=
NM_022725.3:c.868C= , LRG_527t1:c.868C= NP_073562.1:p.Gln290=
NM_022725.4:c.868C= MANE Select NP_073562.1:p.Gln290=