Canonical Allele Identifier: CA380058965
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1176707210

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625333C>A , CM000673.2:g.22625333C>A GRCh38
NC_000011.9:g.22646879C>A , CM000673.1:g.22646879C>A GRCh37
NC_000011.8:g.22603455C>A NCBI36
NG_007425.1:g.5509G>T , LRG_527:g.5509G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.478G>T MANE Select ENSP00000330875.3:p.Asp160Tyr
ENST00000327470.4:c.478G>T ENSP00000330875.3:p.Asp160Tyr
NM_022725.3:c.478G>T , LRG_527t1:c.478G>T NP_073562.1:p.Asp160Tyr
NM_022725.4:c.478G>T MANE Select NP_073562.1:p.Asp160Tyr