Canonical Allele Identifier: CA1217761795

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196727677T= , CM000663.2:g.196727677T=	GRCh38
NC_000001.10:g.196696807T= , CM000663.1:g.196696807T=	GRCh37
NC_000001.9:g.194963430T=	NCBI36
NG_007259.1:g.80667T= , LRG_47:g.80667T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.2503-669T=
ENST00000695969.1:c.2237-669T=	ENSP00000512296.1:n.2237-669T=
ENST00000695970.1:c.2237-669T=	ENSP00000512297.1:n.2237-669T=
ENST00000695971.1:c.2216-669T=	ENSP00000512298.1:n.2216-669T=
ENST00000695972.1:c.2232+741T=	ENSP00000512299.1:n.2232+741T=
ENST00000695973.1:c.*601-669T=	ENSP00000512300.1:n.*601-669T=
ENST00000695974.1:c.2060-669T=	ENSP00000512301.1:n.2060-669T=
ENST00000695975.1:c.*364-669T=	ENSP00000512302.1:n.*364-669T=
ENST00000695976.1:c.2048-669T=	ENSP00000512303.1:n.2048-669T=
ENST00000695981.1:c.2237-669T=	ENSP00000512306.1:n.2237-669T=
ENST00000695983.1:c.2237-669T=	ENSP00000512308.1:n.2237-669T=
ENST00000695984.1:c.245-669T=	ENSP00000512309.1:n.245-669T=
ENST00000695986.1:c.*1888-669T=	ENSP00000512311.1:n.*1888-669T=
ENST00000696025.1:n.2321-669T=
ENST00000696026.1:c.*519-669T=	ENSP00000512335.1:n.*519-669T=
ENST00000696027.1:c.2237-675T=	ENSP00000512336.1:n.2237-675T=
ENST00000696028.1:c.2237-669T=	ENSP00000512337.1:n.2237-669T=
ENST00000696029.1:c.2237-669T=	ENSP00000512338.1:n.2237-669T=
ENST00000696031.1:c.*1755-669T=	ENSP00000512340.1:n.*1755-669T=
ENST00000696032.1:c.2237-669T=	ENSP00000512341.1:n.2237-669T=
ENST00000696033.1:c.1159+38063T=	ENSP00000512342.1:n.1159+38063T=
ENST00000367429.9:c.2237-669T= MANE Select	ENSP00000356399.4:n.2237-669T=
ENST00000367429.8:c.2237-669T=	ENSP00000356399.4:n.2237-669T=
ENST00000466229.5:n.4253-669T=
NM_000186.3:c.2237-669T= , LRG_47t1:c.2237-669T=	NP_000177.2:n.2237-669T=
XR_001737134.2:n.2423-669T=
NM_000186.4:c.2237-669T= MANE Select	NP_000177.2:n.2237-669T=