Canonical Allele Identifier: CA2580082866
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2445706
ClinVar RCV Id: RCV003155625
gnomAD v4: 11-22625155-TGG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625158_22625159del , CM000673.2:g.22625158_22625159del GRCh38
NC_000011.9:g.22646704_22646705del , CM000673.1:g.22646704_22646705del GRCh37
NC_000011.8:g.22603280_22603281del NCBI36
NG_007425.1:g.5685_5686del , LRG_527:g.5685_5686del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.654_655del MANE Select ENSP00000330875.3:p.Gln219ArgfsTer?
ENST00000327470.4:c.654_655del ENSP00000330875.3:p.Gln219ArgfsTer?
NM_022725.3:c.654_655del , LRG_527t1:c.654_655del NP_073562.1:p.Gln219ArgfsTer?
NM_022725.4:c.654_655del MANE Select NP_073562.1:p.Gln219ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'