Canonical Allele Identifier: CA1217761886

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196727766G= , CM000663.2:g.196727766G=	GRCh38
NC_000001.10:g.196696896G= , CM000663.1:g.196696896G=	GRCh37
NC_000001.9:g.194963519G=	NCBI36
NG_007259.1:g.80756G= , LRG_47:g.80756G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.2503-580G=
ENST00000695969.1:c.2237-580G=	ENSP00000512296.1:n.2237-580G=
ENST00000695970.1:c.2237-580G=	ENSP00000512297.1:n.2237-580G=
ENST00000695971.1:c.2216-580G=	ENSP00000512298.1:n.2216-580G=
ENST00000695972.1:c.2232+830G=	ENSP00000512299.1:n.2232+830G=
ENST00000695973.1:c.*601-580G=	ENSP00000512300.1:n.*601-580G=
ENST00000695974.1:c.2060-580G=	ENSP00000512301.1:n.2060-580G=
ENST00000695975.1:c.*364-580G=	ENSP00000512302.1:n.*364-580G=
ENST00000695976.1:c.2048-580G=	ENSP00000512303.1:n.2048-580G=
ENST00000695981.1:c.2237-580G=	ENSP00000512306.1:n.2237-580G=
ENST00000695983.1:c.2237-580G=	ENSP00000512308.1:n.2237-580G=
ENST00000695984.1:c.245-580G=	ENSP00000512309.1:n.245-580G=
ENST00000695986.1:c.*1888-580G=	ENSP00000512311.1:n.*1888-580G=
ENST00000696025.1:n.2321-580G=
ENST00000696026.1:c.*519-580G=	ENSP00000512335.1:n.*519-580G=
ENST00000696027.1:c.2237-586G=	ENSP00000512336.1:n.2237-586G=
ENST00000696028.1:c.2237-580G=	ENSP00000512337.1:n.2237-580G=
ENST00000696029.1:c.2237-580G=	ENSP00000512338.1:n.2237-580G=
ENST00000696031.1:c.*1755-580G=	ENSP00000512340.1:n.*1755-580G=
ENST00000696032.1:c.2237-580G=	ENSP00000512341.1:n.2237-580G=
ENST00000696033.1:c.1159+38152G=	ENSP00000512342.1:n.1159+38152G=
ENST00000367429.9:c.2237-580G= MANE Select	ENSP00000356399.4:n.2237-580G=
ENST00000367429.8:c.2237-580G=	ENSP00000356399.4:n.2237-580G=
ENST00000466229.5:n.4253-580G=
NM_000186.3:c.2237-580G= , LRG_47t1:c.2237-580G=	NP_000177.2:n.2237-580G=
XR_001737134.2:n.2423-580G=
NM_000186.4:c.2237-580G= MANE Select	NP_000177.2:n.2237-580G=