Canonical Allele Identifier: CA219086641
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1029647387
gnomAD v4: 11-22625356-C-T
COSMIC: COSM5473118
MyVariant Identifiers: chr11:g.22646902C>T (hg19) chr11:g.22625356C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625356C>T , CM000673.2:g.22625356C>T GRCh38
NC_000011.9:g.22646902C>T , CM000673.1:g.22646902C>T GRCh37
NC_000011.8:g.22603478C>T NCBI36
NG_007425.1:g.5486G>A , LRG_527:g.5486G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.455G>A MANE Select ENSP00000330875.3:p.Arg152Lys
ENST00000327470.4:c.455G>A ENSP00000330875.3:p.Arg152Lys
NM_022725.3:c.455G>A , LRG_527t1:c.455G>A NP_073562.1:p.Arg152Lys
NM_022725.4:c.455G>A MANE Select NP_073562.1:p.Arg152Lys
Search 100 bp 5'
Search 100 bp 3'