Canonical Allele Identifier: CA5924232
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 964280
dbSNP Id: rs372140217

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624900C>G , CM000673.2:g.22624900C>G GRCh38
NC_000011.9:g.22646446C>G , CM000673.1:g.22646446C>G GRCh37
NC_000011.8:g.22603022C>G NCBI36
NG_007425.1:g.5942G>C , LRG_527:g.5942G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.911G>C MANE Select ENSP00000330875.3:p.Trp304Ser
ENST00000327470.4:c.911G>C ENSP00000330875.3:p.Trp304Ser
NM_022725.3:c.911G>C , LRG_527t1:c.911G>C NP_073562.1:p.Trp304Ser
NM_022725.4:c.911G>C MANE Select NP_073562.1:p.Trp304Ser