Canonical Allele Identifier: CA1957607125
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625287T= , CM000673.2:g.22625287T= GRCh38
NC_000011.9:g.22646833T= , CM000673.1:g.22646833T= GRCh37
NC_000011.8:g.22603409T= NCBI36
NG_007425.1:g.5555A= , LRG_527:g.5555A=

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.524A= MANE Select ENSP00000330875.3:p.Gln175=
ENST00000327470.4:c.524A= ENSP00000330875.3:p.Gln175=
NM_022725.3:c.524A= , LRG_527t1:c.524A= NP_073562.1:p.Gln175=
NM_022725.4:c.524A= MANE Select NP_073562.1:p.Gln175=