Canonical Allele Identifier: CA2612850461
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625014-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625016del , CM000673.2:g.22625016del GRCh38
NC_000011.9:g.22646562del , CM000673.1:g.22646562del GRCh37
NC_000011.8:g.22603138del NCBI36
NG_007425.1:g.5827del , LRG_527:g.5827del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.796del MANE Select ENSP00000330875.3:p.Arg266AlafsTer13
ENST00000327470.4:c.796del ENSP00000330875.3:p.Arg266AlafsTer13
NM_022725.3:c.796del , LRG_527t1:c.796del NP_073562.1:p.Arg266AlafsTer13
NM_022725.4:c.796del MANE Select NP_073562.1:p.Arg266AlafsTer13
Search 100 bp 5'
Search 100 bp 3'