Canonical Allele Identifier: CA1143382368

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517265C= , CM000663.2:g.241517265C=	GRCh38
NC_000001.10:g.241680565C= , CM000663.1:g.241680565C=	GRCh37
NC_000001.9:g.239747188C=	NCBI36
NG_012338.1:g.7490G= , LRG_504:g.7490G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.687G=
ENST00000682162.1:c.213G=	ENSP00000508203.1:n.213G=
ENST00000682567.1:n.261G=
ENST00000683521.1:c.184G=	ENSP00000506864.1:p.Val62=
ENST00000684483.1:c.184G=	ENSP00000507894.1:p.Val62=
ENST00000366560.4:c.184G= MANE Select	ENSP00000355518.4:p.Val62=
ENST00000366560.3:c.184G=	ENSP00000355518.3:p.Val62=
ENST00000493477.1:n.297G=
NM_000143.3:c.184G= , LRG_504t1:c.184G=	NP_000134.2:p.Val62=
XM_011544132.1:c.-45G=	XP_011542434.1:n.-45G=
XM_011544132.2:c.-45G=	XP_011542434.1:n.-45G=
NM_000143.4:c.184G= MANE Select	NP_000134.2:p.Val62=