Canonical Allele Identifier: CA380058557
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1346671180

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625135T>C , CM000673.2:g.22625135T>C GRCh38
NC_000011.9:g.22646681T>C , CM000673.1:g.22646681T>C GRCh37
NC_000011.8:g.22603257T>C NCBI36
NG_007425.1:g.5707A>G , LRG_527:g.5707A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.676A>G MANE Select ENSP00000330875.3:p.Ile226Val
ENST00000327470.4:c.676A>G ENSP00000330875.3:p.Ile226Val
NM_022725.3:c.676A>G , LRG_527t1:c.676A>G NP_073562.1:p.Ile226Val
NM_022725.4:c.676A>G MANE Select NP_073562.1:p.Ile226Val