Canonical Allele Identifier: CA380058651
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625182A>G , CM000673.2:g.22625182A>G GRCh38
NC_000011.9:g.22646728A>G , CM000673.1:g.22646728A>G GRCh37
NC_000011.8:g.22603304A>G NCBI36
NG_007425.1:g.5660T>C , LRG_527:g.5660T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.629T>C MANE Select ENSP00000330875.3:p.Leu210Ser
ENST00000327470.4:c.629T>C ENSP00000330875.3:p.Leu210Ser
NM_022725.3:c.629T>C , LRG_527t1:c.629T>C NP_073562.1:p.Leu210Ser
NM_022725.4:c.629T>C MANE Select NP_073562.1:p.Leu210Ser