Canonical Allele Identifier: CA1957581347
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625473T= , CM000673.2:g.22625473T= GRCh38
NC_000011.9:g.22647019T= , CM000673.1:g.22647019T= GRCh37
NC_000011.8:g.22603595T= NCBI36
NG_007425.1:g.5369A= , LRG_527:g.5369A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.338A= MANE Select ENSP00000330875.3:p.Gln113=
ENST00000327470.4:c.338A= ENSP00000330875.3:p.Gln113=
NM_022725.3:c.338A= , LRG_527t1:c.338A= NP_073562.1:p.Gln113=
NM_022725.4:c.338A= MANE Select NP_073562.1:p.Gln113=
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