Canonical Allele Identifier: CA473533783
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1528426
ClinVar RCV Id: RCV002071253
dbSNP Id: rs2133797216
gnomAD v4: 11-22625166-A-T
MyVariant Identifiers: chr11:g.22646712A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625166A>T , CM000673.2:g.22625166A>T GRCh38
NC_000011.9:g.22646712A>T , CM000673.1:g.22646712A>T GRCh37
NC_000011.8:g.22603288A>T NCBI36
NG_007425.1:g.5676T>A , LRG_527:g.5676T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.645T>A MANE Select ENSP00000330875.3:p.Ser215=
ENST00000327470.4:c.645T>A ENSP00000330875.3:p.Ser215=
NM_022725.3:c.645T>A , LRG_527t1:c.645T>A NP_073562.1:p.Ser215=
NM_022725.4:c.645T>A MANE Select NP_073562.1:p.Ser215=
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Search 100 bp 3'