Canonical Allele Identifier: CA2612850468
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625331-GTCC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625336_22625338del , CM000673.2:g.22625336_22625338del GRCh38
NC_000011.9:g.22646882_22646884del , CM000673.1:g.22646882_22646884del GRCh37
NC_000011.8:g.22603458_22603460del NCBI36
NG_007425.1:g.5508_5510del , LRG_527:g.5508_5510del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.477_479del MANE Select ENSP00000330875.3:p.Glu159del
ENST00000327470.4:c.477_479del ENSP00000330875.3:p.Glu159del
NM_022725.3:c.477_479del , LRG_527t1:c.477_479del NP_073562.1:p.Glu159del
NM_022725.4:c.477_479del MANE Select NP_073562.1:p.Glu159del
Search 100 bp 5'
Search 100 bp 3'