Canonical Allele Identifier: CA380058553
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs2133797091

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625133G>C , CM000673.2:g.22625133G>C GRCh38
NC_000011.9:g.22646679G>C , CM000673.1:g.22646679G>C GRCh37
NC_000011.8:g.22603255G>C NCBI36
NG_007425.1:g.5709C>G , LRG_527:g.5709C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.678C>G MANE Select ENSP00000330875.3:p.Ile226Met
ENST00000327470.4:c.678C>G ENSP00000330875.3:p.Ile226Met
NM_022725.3:c.678C>G , LRG_527t1:c.678C>G NP_073562.1:p.Ile226Met
NM_022725.4:c.678C>G MANE Select NP_073562.1:p.Ile226Met