Canonical Allele Identifier: CA380058957
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625330A>C , CM000673.2:g.22625330A>C GRCh38
NC_000011.9:g.22646876A>C , CM000673.1:g.22646876A>C GRCh37
NC_000011.8:g.22603452A>C NCBI36
NG_007425.1:g.5512T>G , LRG_527:g.5512T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.481T>G MANE Select ENSP00000330875.3:p.Ser161Ala
ENST00000327470.4:c.481T>G ENSP00000330875.3:p.Ser161Ala
NM_022725.3:c.481T>G , LRG_527t1:c.481T>G NP_073562.1:p.Ser161Ala
NM_022725.4:c.481T>G MANE Select NP_073562.1:p.Ser161Ala