Canonical Allele Identifier: CA219086645
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1373268
ClinVar RCV Id: RCV001880709 RCV002482587
dbSNP Id: rs868692458
gnomAD v4: 11-22625392-C-T
MyVariant Identifiers: chr11:g.22646938C>T (hg19) chr11:g.22625392C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625392C>T , CM000673.2:g.22625392C>T GRCh38
NC_000011.9:g.22646938C>T , CM000673.1:g.22646938C>T GRCh37
NC_000011.8:g.22603514C>T NCBI36
NG_007425.1:g.5450G>A , LRG_527:g.5450G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.419G>A MANE Select ENSP00000330875.3:p.Arg140Gln
ENST00000327470.4:c.419G>A ENSP00000330875.3:p.Arg140Gln
NM_022725.3:c.419G>A , LRG_527t1:c.419G>A NP_073562.1:p.Arg140Gln
NM_022725.4:c.419G>A MANE Select NP_073562.1:p.Arg140Gln
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Search 100 bp 3'