Canonical Allele Identifier: CA1957606928
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624930C= , CM000673.2:g.22624930C= GRCh38
NC_000011.9:g.22646476C= , CM000673.1:g.22646476C= GRCh37
NC_000011.8:g.22603052C= NCBI36
NG_007425.1:g.5912G= , LRG_527:g.5912G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.881G= MANE Select ENSP00000330875.3:p.Trp294=
ENST00000327470.4:c.881G= ENSP00000330875.3:p.Trp294=
NM_022725.3:c.881G= , LRG_527t1:c.881G= NP_073562.1:p.Trp294=
NM_022725.4:c.881G= MANE Select NP_073562.1:p.Trp294=
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