Canonical Allele Identifier: CA1957606926
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624928C= , CM000673.2:g.22624928C= GRCh38
NC_000011.9:g.22646474C= , CM000673.1:g.22646474C= GRCh37
NC_000011.8:g.22603050C= NCBI36
NG_007425.1:g.5914G= , LRG_527:g.5914G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.883G= MANE Select ENSP00000330875.3:p.Val295=
ENST00000327470.4:c.883G= ENSP00000330875.3:p.Val295=
NM_022725.3:c.883G= , LRG_527t1:c.883G= NP_073562.1:p.Val295=
NM_022725.4:c.883G= MANE Select NP_073562.1:p.Val295=
Search 100 bp 5'
Search 100 bp 3'