Canonical Allele Identifier: CA1229584115

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517248A= , CM000663.2:g.241517248A=	GRCh38
NC_000001.10:g.241680548A= , CM000663.1:g.241680548A=	GRCh37
NC_000001.9:g.239747171A=	NCBI36
NG_012338.1:g.7507T= , LRG_504:g.7507T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.704T=
ENST00000682162.1:c.230T=	ENSP00000508203.1:n.230T=
ENST00000682567.1:n.278T=
ENST00000683521.1:c.201T=	ENSP00000506864.1:p.Tyr67=
ENST00000684483.1:c.201T=	ENSP00000507894.1:p.Tyr67=
ENST00000366560.4:c.201T= MANE Select	ENSP00000355518.4:p.Tyr67=
ENST00000366560.3:c.201T=	ENSP00000355518.3:p.Tyr67=
ENST00000493477.1:n.314T=
NM_000143.3:c.201T= , LRG_504t1:c.201T=	NP_000134.2:p.Tyr67=
XM_011544132.1:c.-28T=	XP_011542434.1:n.-28T=
XM_011544132.2:c.-28T=	XP_011542434.1:n.-28T=
NM_000143.4:c.201T= MANE Select	NP_000134.2:p.Tyr67=