Canonical Allele Identifier: CA1229581899

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241511708C= , CM000663.2:g.241511708C=	GRCh38
NC_000001.10:g.241675008C= , CM000663.1:g.241675008C=	GRCh37
NC_000001.9:g.239741631C=	NCBI36
NG_012338.1:g.13047G= , LRG_504:g.13047G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1058+259G=
ENST00000682162.1:c.584+259G=	ENSP00000508203.1:n.584+259G=
ENST00000682567.1:n.632+259G=
ENST00000683521.1:c.555+259G=	ENSP00000506864.1:n.555+259G=
ENST00000684483.1:c.555+259G=	ENSP00000507894.1:n.555+259G=
ENST00000366560.4:c.555+259G= MANE Select	ENSP00000355518.4:n.555+259G=
ENST00000366560.3:c.555+259G=	ENSP00000355518.3:n.555+259G=
NM_000143.3:c.555+259G= , LRG_504t1:c.555+259G=	NP_000134.2:n.555+259G=
XM_011544132.1:c.327+259G=	XP_011542434.1:n.327+259G=
XM_011544132.2:c.327+259G=	XP_011542434.1:n.327+259G=
NM_000143.4:c.555+259G= MANE Select	NP_000134.2:n.555+259G=