Canonical Allele Identifier: CA1957606985
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625038C= , CM000673.2:g.22625038C= GRCh38
NC_000011.9:g.22646584C= , CM000673.1:g.22646584C= GRCh37
NC_000011.8:g.22603160C= NCBI36
NG_007425.1:g.5804G= , LRG_527:g.5804G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.773G= MANE Select ENSP00000330875.3:p.Gly258=
ENST00000327470.4:c.773G= ENSP00000330875.3:p.Gly258=
NM_022725.3:c.773G= , LRG_527t1:c.773G= NP_073562.1:p.Gly258=
NM_022725.4:c.773G= MANE Select NP_073562.1:p.Gly258=