Canonical Allele Identifier: CA380059184
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1590541791

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625440G>A , CM000673.2:g.22625440G>A GRCh38
NC_000011.9:g.22646986G>A , CM000673.1:g.22646986G>A GRCh37
NC_000011.8:g.22603562G>A NCBI36
NG_007425.1:g.5402C>T , LRG_527:g.5402C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.371C>T MANE Select ENSP00000330875.3:p.Ala124Val
ENST00000327470.4:c.371C>T ENSP00000330875.3:p.Ala124Val
NM_022725.3:c.371C>T , LRG_527t1:c.371C>T NP_073562.1:p.Ala124Val
NM_022725.4:c.371C>T MANE Select NP_073562.1:p.Ala124Val