Canonical Allele Identifier: CA380059201
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1858630528

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625449A>T , CM000673.2:g.22625449A>T GRCh38
NC_000011.9:g.22646995A>T , CM000673.1:g.22646995A>T GRCh37
NC_000011.8:g.22603571A>T NCBI36
NG_007425.1:g.5393T>A , LRG_527:g.5393T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.362T>A MANE Select ENSP00000330875.3:p.Val121Asp
ENST00000327470.4:c.362T>A ENSP00000330875.3:p.Val121Asp
NM_022725.3:c.362T>A , LRG_527t1:c.362T>A NP_073562.1:p.Val121Asp
NM_022725.4:c.362T>A MANE Select NP_073562.1:p.Val121Asp