Canonical Allele Identifier: CA380058144
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624933A>G , CM000673.2:g.22624933A>G GRCh38
NC_000011.9:g.22646479A>G , CM000673.1:g.22646479A>G GRCh37
NC_000011.8:g.22603055A>G NCBI36
NG_007425.1:g.5909T>C , LRG_527:g.5909T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.878T>C MANE Select ENSP00000330875.3:p.Ile293Thr
ENST00000327470.4:c.878T>C ENSP00000330875.3:p.Ile293Thr
NM_022725.3:c.878T>C , LRG_527t1:c.878T>C NP_073562.1:p.Ile293Thr
NM_022725.4:c.878T>C MANE Select NP_073562.1:p.Ile293Thr