Canonical Allele Identifier: CA2573975565

Gene: CFH

Linked Data

• gnomAD v4: 1-196747386-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747386A>G , CM000663.2:g.196747386A>G	GRCh38
NC_000001.10:g.196716516A>G , CM000663.1:g.196716516A>G	GRCh37
NC_000001.9:g.194983139A>G	NCBI36
NG_007259.1:g.100376A>G , LRG_47:g.100376A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4797A>G
ENST00000695970.1:c.*73A>G	ENSP00000512297.1:n.*73A>G
ENST00000695971.1:c.*73A>G	ENSP00000512298.1:n.*73A>G
ENST00000695972.1:c.*846A>G	ENSP00000512299.1:n.*846A>G
ENST00000695973.1:c.*2133A>G	ENSP00000512300.1:n.*2133A>G
ENST00000695974.1:c.*73A>G	ENSP00000512301.1:n.*73A>G
ENST00000695975.1:c.*1896A>G	ENSP00000512302.1:n.*1896A>G
ENST00000695976.1:c.*73A>G	ENSP00000512303.1:n.*73A>G
ENST00000695981.1:c.3580+189A>G	ENSP00000512306.1:n.3580+189A>G
ENST00000695984.1:c.*73A>G	ENSP00000512309.1:n.*73A>G
ENST00000695986.1:c.*3420A>G	ENSP00000512311.1:n.*3420A>G
ENST00000695990.1:n.803A>G
ENST00000696026.1:c.*2051A>G	ENSP00000512335.1:n.*2051A>G
ENST00000696027.1:c.*73A>G	ENSP00000512336.1:n.*73A>G
ENST00000696028.1:c.*73A>G	ENSP00000512337.1:n.*73A>G
ENST00000696029.1:c.*73A>G	ENSP00000512338.1:n.*73A>G
ENST00000696031.1:c.*3287A>G	ENSP00000512340.1:n.*3287A>G
ENST00000696032.1:c.3580+189A>G	ENSP00000512341.1:n.3580+189A>G
ENST00000696033.1:c.1160-32411A>G	ENSP00000512342.1:n.1160-32411A>G
ENST00000367429.9:c.*73A>G MANE Select	ENSP00000356399.4:n.*73A>G
ENST00000367429.8:c.*73A>G	ENSP00000356399.4:n.*73A>G
ENST00000466229.5:n.6867A>G
NM_000186.3:c.*73A>G , LRG_47t1:c.*73A>G	NP_000177.2:n.*73A>G
XR_001737134.2:n.3955A>G
NM_000186.4:c.*73A>G MANE Select	NP_000177.2:n.*73A>G