Canonical Allele Identifier: CA473533392
Gene: FANCF HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22646469T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624923T>C , CM000673.2:g.22624923T>C GRCh38
NC_000011.9:g.22646469T>C , CM000673.1:g.22646469T>C GRCh37
NC_000011.8:g.22603045T>C NCBI36
NG_007425.1:g.5919A>G , LRG_527:g.5919A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.888A>G MANE Select ENSP00000330875.3:p.Gly296=
ENST00000327470.4:c.888A>G ENSP00000330875.3:p.Gly296=
NM_022725.3:c.888A>G , LRG_527t1:c.888A>G NP_073562.1:p.Gly296=
NM_022725.4:c.888A>G MANE Select NP_073562.1:p.Gly296=
Search 100 bp 5'
Search 100 bp 3'