Canonical Allele Identifier: CA1229580771

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508934A= , CM000663.2:g.241508934A=	GRCh38
NC_000001.10:g.241672234A= , CM000663.1:g.241672234A=	GRCh37
NC_000001.9:g.239738857A=	NCBI36
NG_012338.1:g.15821T= , LRG_504:g.15821T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-149T=
ENST00000682162.1:c.585-149T=	ENSP00000508203.1:n.585-149T=
ENST00000682567.1:n.633-149T=
ENST00000683521.1:c.556-149T=	ENSP00000506864.1:n.556-149T=
ENST00000684161.1:n.1622T=
ENST00000684483.1:c.556-174T=	ENSP00000507894.1:n.556-174T=
ENST00000366560.4:c.556-149T= MANE Select	ENSP00000355518.4:n.556-149T=
ENST00000366560.3:c.556-149T=	ENSP00000355518.3:n.556-149T=
NM_000143.3:c.556-149T= , LRG_504t1:c.556-149T=	NP_000134.2:n.556-149T=
XM_011544132.1:c.328-149T=	XP_011542434.1:n.328-149T=
XM_011544132.2:c.328-149T=	XP_011542434.1:n.328-149T=
NM_000143.4:c.556-149T= MANE Select	NP_000134.2:n.556-149T=