Canonical Allele Identifier: CA380059085
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1590541679

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625390A>C , CM000673.2:g.22625390A>C GRCh38
NC_000011.9:g.22646936A>C , CM000673.1:g.22646936A>C GRCh37
NC_000011.8:g.22603512A>C NCBI36
NG_007425.1:g.5452T>G , LRG_527:g.5452T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.421T>G MANE Select ENSP00000330875.3:p.Ser141Ala
ENST00000327470.4:c.421T>G ENSP00000330875.3:p.Ser141Ala
NM_022725.3:c.421T>G , LRG_527t1:c.421T>G NP_073562.1:p.Ser141Ala
NM_022725.4:c.421T>G MANE Select NP_073562.1:p.Ser141Ala