Canonical Allele Identifier: CA1957606942

Gene: FANCF

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22624967C= , CM000673.2:g.22624967C=	GRCh38
NC_000011.9:g.22646513C= , CM000673.1:g.22646513C=	GRCh37
NC_000011.8:g.22603089C=	NCBI36
NG_007425.1:g.5875G= , LRG_527:g.5875G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327470.6:c.844G= MANE Select	ENSP00000330875.3:p.Gly282=
ENST00000327470.4:c.844G=	ENSP00000330875.3:p.Gly282=
NM_022725.3:c.844G= , LRG_527t1:c.844G=	NP_073562.1:p.Gly282=
NM_022725.4:c.844G= MANE Select	NP_073562.1:p.Gly282=