Canonical Allele Identifier: CA2649647365

Gene: CFH

Linked Data

• gnomAD v4: 1-196747478-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747478G>A , CM000663.2:g.196747478G>A	GRCh38
NC_000001.10:g.196716608G>A , CM000663.1:g.196716608G>A	GRCh37
NC_000001.9:g.194983231G>A	NCBI36
NG_007259.1:g.100468G>A , LRG_47:g.100468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4889G>A
ENST00000695970.1:c.*165G>A	ENSP00000512297.1:n.*165G>A
ENST00000695971.1:c.*165G>A	ENSP00000512298.1:n.*165G>A
ENST00000695972.1:c.*938G>A	ENSP00000512299.1:n.*938G>A
ENST00000695973.1:c.*2225G>A	ENSP00000512300.1:n.*2225G>A
ENST00000695974.1:c.*165G>A	ENSP00000512301.1:n.*165G>A
ENST00000695975.1:c.*1988G>A	ENSP00000512302.1:n.*1988G>A
ENST00000695976.1:c.*165G>A	ENSP00000512303.1:n.*165G>A
ENST00000695981.1:c.3580+281G>A	ENSP00000512306.1:n.3580+281G>A
ENST00000695984.1:c.*165G>A	ENSP00000512309.1:n.*165G>A
ENST00000695986.1:c.*3512G>A	ENSP00000512311.1:n.*3512G>A
ENST00000695990.1:n.895G>A
ENST00000696026.1:c.*2143G>A	ENSP00000512335.1:n.*2143G>A
ENST00000696027.1:c.*165G>A	ENSP00000512336.1:n.*165G>A
ENST00000696028.1:c.*165G>A	ENSP00000512337.1:n.*165G>A
ENST00000696029.1:c.*165G>A	ENSP00000512338.1:n.*165G>A
ENST00000696031.1:c.*3379G>A	ENSP00000512340.1:n.*3379G>A
ENST00000696032.1:c.3580+281G>A	ENSP00000512341.1:n.3580+281G>A
ENST00000696033.1:c.1160-32319G>A	ENSP00000512342.1:n.1160-32319G>A
ENST00000367429.9:c.*165G>A MANE Select	ENSP00000356399.4:n.*165G>A
ENST00000367429.8:c.*165G>A	ENSP00000356399.4:n.*165G>A
ENST00000466229.5:n.6959G>A
NM_000186.3:c.*165G>A , LRG_47t1:c.*165G>A	NP_000177.2:n.*165G>A
XR_001737134.2:n.4047G>A
NM_000186.4:c.*165G>A MANE Select	NP_000177.2:n.*165G>A