Canonical Allele Identifier: CA473533705
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1099619
ClinVar RCV Id: RCV001421951
dbSNP Id: rs1565055031
gnomAD v2: 11-22646658-C-T
gnomAD v3: 11-22625112-C-T
gnomAD v4: 11-22625112-C-T
MyVariant Identifiers: chr11:g.22646658C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625112C>T , CM000673.2:g.22625112C>T GRCh38
NC_000011.9:g.22646658C>T , CM000673.1:g.22646658C>T GRCh37
NC_000011.8:g.22603234C>T NCBI36
NG_007425.1:g.5730G>A , LRG_527:g.5730G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.699G>A MANE Select ENSP00000330875.3:p.Gly233=
ENST00000327470.4:c.699G>A ENSP00000330875.3:p.Gly233=
NM_022725.3:c.699G>A , LRG_527t1:c.699G>A NP_073562.1:p.Gly233=
NM_022725.4:c.699G>A MANE Select NP_073562.1:p.Gly233=
Search 100 bp 5'
Search 100 bp 3'