Canonical Allele Identifier: CA1957606939

Gene: FANCF

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22624954T= , CM000673.2:g.22624954T=	GRCh38
NC_000011.9:g.22646500T= , CM000673.1:g.22646500T=	GRCh37
NC_000011.8:g.22603076T=	NCBI36
NG_007425.1:g.5888A= , LRG_527:g.5888A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327470.6:c.857A= MANE Select	ENSP00000330875.3:p.His286=
ENST00000327470.4:c.857A=	ENSP00000330875.3:p.His286=
NM_022725.3:c.857A= , LRG_527t1:c.857A=	NP_073562.1:p.His286=
NM_022725.4:c.857A= MANE Select	NP_073562.1:p.His286=