Canonical Allele Identifier: CA380059254
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1858631294

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625477C>G , CM000673.2:g.22625477C>G GRCh38
NC_000011.9:g.22647023C>G , CM000673.1:g.22647023C>G GRCh37
NC_000011.8:g.22603599C>G NCBI36
NG_007425.1:g.5365G>C , LRG_527:g.5365G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.334G>C MANE Select ENSP00000330875.3:p.Val112Leu
ENST00000327470.4:c.334G>C ENSP00000330875.3:p.Val112Leu
NM_022725.3:c.334G>C , LRG_527t1:c.334G>C NP_073562.1:p.Val112Leu
NM_022725.4:c.334G>C MANE Select NP_073562.1:p.Val112Leu