Canonical Allele Identifier: CA380059264
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625483G>T , CM000673.2:g.22625483G>T GRCh38
NC_000011.9:g.22647029G>T , CM000673.1:g.22647029G>T GRCh37
NC_000011.8:g.22603605G>T NCBI36
NG_007425.1:g.5359C>A , LRG_527:g.5359C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.328C>A MANE Select ENSP00000330875.3:p.His110Asn
ENST00000327470.4:c.328C>A ENSP00000330875.3:p.His110Asn
NM_022725.3:c.328C>A , LRG_527t1:c.328C>A NP_073562.1:p.His110Asn
NM_022725.4:c.328C>A MANE Select NP_073562.1:p.His110Asn