Canonical Allele Identifier: CA380059166
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1277670335

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625432C>T , CM000673.2:g.22625432C>T GRCh38
NC_000011.9:g.22646978C>T , CM000673.1:g.22646978C>T GRCh37
NC_000011.8:g.22603554C>T NCBI36
NG_007425.1:g.5410G>A , LRG_527:g.5410G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.379G>A MANE Select ENSP00000330875.3:p.Glu127Lys
ENST00000327470.4:c.379G>A ENSP00000330875.3:p.Glu127Lys
NM_022725.3:c.379G>A , LRG_527t1:c.379G>A NP_073562.1:p.Glu127Lys
NM_022725.4:c.379G>A MANE Select NP_073562.1:p.Glu127Lys