Canonical Allele Identifier: CA1217758353

Gene: CFH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196724252G= , CM000663.2:g.196724252G=	GRCh38
NC_000001.10:g.196693382G= , CM000663.1:g.196693382G=	GRCh37
NC_000001.9:g.194960005G=	NCBI36
NG_007259.1:g.77242G= , LRG_47:g.77242G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.1963-869G=
ENST00000695969.1:c.1697-869G=	ENSP00000512296.1:n.1697-869G=
ENST00000695970.1:c.1697-869G=	ENSP00000512297.1:n.1697-869G=
ENST00000695971.1:c.1676-869G=	ENSP00000512298.1:n.1676-869G=
ENST00000695972.1:c.1697-869G=	ENSP00000512299.1:n.1697-869G=
ENST00000695973.1:c.*61-869G=	ENSP00000512300.1:n.*61-869G=
ENST00000695974.1:c.1697-2218G=	ENSP00000512301.1:n.1697-2218G=
ENST00000695975.1:c.1697-869G=	ENSP00000512302.1:n.1697-869G=
ENST00000695976.1:c.1508-869G=	ENSP00000512303.1:n.1508-869G=
ENST00000695981.1:c.1697-869G=	ENSP00000512306.1:n.1697-869G=
ENST00000695983.1:c.1697-869G=	ENSP00000512308.1:n.1697-869G=
ENST00000695984.1:c.245-4094G=	ENSP00000512309.1:n.245-4094G=
ENST00000695986.1:c.*1348-869G=	ENSP00000512311.1:n.*1348-869G=
ENST00000696025.1:n.1781-869G=
ENST00000696026.1:c.1701-875G=	ENSP00000512335.1:n.1701-875G=
ENST00000696027.1:c.1697-869G=	ENSP00000512336.1:n.1697-869G=
ENST00000696028.1:c.1697-869G=	ENSP00000512337.1:n.1697-869G=
ENST00000696029.1:c.1697-869G=	ENSP00000512338.1:n.1697-869G=
ENST00000696031.1:c.*1215-869G=	ENSP00000512340.1:n.*1215-869G=
ENST00000696032.1:c.1697-869G=	ENSP00000512341.1:n.1697-869G=
ENST00000696033.1:c.1159+34638G=	ENSP00000512342.1:n.1159+34638G=
ENST00000367429.9:c.1697-869G= MANE Select	ENSP00000356399.4:n.1697-869G=
ENST00000367429.8:c.1697-869G=	ENSP00000356399.4:n.1697-869G=
ENST00000466229.5:n.3713-869G=
NM_000186.3:c.1697-869G= , LRG_47t1:c.1697-869G=	NP_000177.2:n.1697-869G=
XR_001737134.2:n.1883-869G=
NM_000186.4:c.1697-869G= MANE Select	NP_000177.2:n.1697-869G=