Canonical Allele Identifier: CA380058837
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625272G>T , CM000673.2:g.22625272G>T GRCh38
NC_000011.9:g.22646818G>T , CM000673.1:g.22646818G>T GRCh37
NC_000011.8:g.22603394G>T NCBI36
NG_007425.1:g.5570C>A , LRG_527:g.5570C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.539C>A MANE Select ENSP00000330875.3:p.Ala180Asp
ENST00000327470.4:c.539C>A ENSP00000330875.3:p.Ala180Asp
NM_022725.3:c.539C>A , LRG_527t1:c.539C>A NP_073562.1:p.Ala180Asp
NM_022725.4:c.539C>A MANE Select NP_073562.1:p.Ala180Asp