Canonical Allele Identifier: CA1229582113

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512178A= , CM000663.2:g.241512178A=	GRCh38
NC_000001.10:g.241675478A= , CM000663.1:g.241675478A=	GRCh37
NC_000001.9:g.239742101A=	NCBI36
NG_012338.1:g.12577T= , LRG_504:g.12577T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.882-35T=
ENST00000682162.1:c.408-35T=	ENSP00000508203.1:n.408-35T=
ENST00000682567.1:n.456-35T=
ENST00000683521.1:c.379-35T=	ENSP00000506864.1:n.379-35T=
ENST00000684483.1:c.379-35T=	ENSP00000507894.1:n.379-35T=
ENST00000366560.4:c.379-35T= MANE Select	ENSP00000355518.4:n.379-35T=
ENST00000366560.3:c.379-35T=	ENSP00000355518.3:n.379-35T=
ENST00000497042.1:n.75-35T=
NM_000143.3:c.379-35T= , LRG_504t1:c.379-35T=	NP_000134.2:n.379-35T=
XM_011544132.1:c.151-35T=	XP_011542434.1:n.151-35T=
XM_011544132.2:c.151-35T=	XP_011542434.1:n.151-35T=
NM_000143.4:c.379-35T= MANE Select	NP_000134.2:n.379-35T=