Canonical Allele Identifier: CA5924252
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 3023096
ClinVar RCV Id: RCV003882282
dbSNP Id: rs771686721
ExAC: 11:22646535 A / G
gnomAD v2: 11-22646535-A-G
gnomAD v4: 11-22624989-A-G
MyVariant Identifiers: chr11:g.22646535A>G (hg19) chr11:g.22624989A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624989A>G , CM000673.2:g.22624989A>G GRCh38
NC_000011.9:g.22646535A>G , CM000673.1:g.22646535A>G GRCh37
NC_000011.8:g.22603111A>G NCBI36
NG_007425.1:g.5853T>C , LRG_527:g.5853T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.822T>C MANE Select ENSP00000330875.3:p.Tyr274=
ENST00000327470.4:c.822T>C ENSP00000330875.3:p.Tyr274=
NM_022725.3:c.822T>C , LRG_527t1:c.822T>C NP_073562.1:p.Tyr274=
NM_022725.4:c.822T>C MANE Select NP_073562.1:p.Tyr274=
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