Canonical Allele Identifier: CA1229578101

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502399A= , CM000663.2:g.241502399A=	GRCh38
NC_000001.10:g.241665699A= , CM000663.1:g.241665699A=	GRCh37
NC_000001.9:g.239732322A=	NCBI36
NG_012338.1:g.22356T= , LRG_504:g.22356T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1739+44T=
ENST00000682162.1:c.1265+44T=	ENSP00000508203.1:n.1265+44T=
ENST00000682567.1:n.2828T=
ENST00000683521.1:c.1236+44T=	ENSP00000506864.1:n.1236+44T=
ENST00000684161.1:n.2451+44T=
ENST00000684483.1:c.*632+44T=	ENSP00000507894.1:n.*632+44T=
ENST00000366560.4:c.1236+44T= MANE Select	ENSP00000355518.4:n.1236+44T=
ENST00000366560.3:c.1236+44T=	ENSP00000355518.3:n.1236+44T=
NM_000143.3:c.1236+44T= , LRG_504t1:c.1236+44T=	NP_000134.2:n.1236+44T=
XM_011544132.1:c.1008+44T=	XP_011542434.1:n.1008+44T=
XM_011544132.2:c.1008+44T=	XP_011542434.1:n.1008+44T=
NM_000143.4:c.1236+44T= MANE Select	NP_000134.2:n.1236+44T=