Canonical Allele Identifier: CA380059266
Gene: FANCF HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22647031T>A (hg19) chr11:g.22625485T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625485T>A , CM000673.2:g.22625485T>A GRCh38
NC_000011.9:g.22647031T>A , CM000673.1:g.22647031T>A GRCh37
NC_000011.8:g.22603607T>A NCBI36
NG_007425.1:g.5357A>T , LRG_527:g.5357A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.326A>T MANE Select ENSP00000330875.3:p.Tyr109Phe
ENST00000327470.4:c.326A>T ENSP00000330875.3:p.Tyr109Phe
NM_022725.3:c.326A>T , LRG_527t1:c.326A>T NP_073562.1:p.Tyr109Phe
NM_022725.4:c.326A>T MANE Select NP_073562.1:p.Tyr109Phe
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