Canonical Allele Identifier: CA380058482
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625098A>T , CM000673.2:g.22625098A>T GRCh38
NC_000011.9:g.22646644A>T , CM000673.1:g.22646644A>T GRCh37
NC_000011.8:g.22603220A>T NCBI36
NG_007425.1:g.5744T>A , LRG_527:g.5744T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.713T>A MANE Select ENSP00000330875.3:p.Val238Asp
ENST00000327470.4:c.713T>A ENSP00000330875.3:p.Val238Asp
NM_022725.3:c.713T>A , LRG_527t1:c.713T>A NP_073562.1:p.Val238Asp
NM_022725.4:c.713T>A MANE Select NP_073562.1:p.Val238Asp