Canonical Allele Identifier: CA343987830
Gene: CFH HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196747203T>A , CM000663.2:g.196747203T>A GRCh38
NC_000001.10:g.196716333T>A , CM000663.1:g.196716333T>A GRCh37
NC_000001.9:g.194982956T>A NCBI36
NG_007259.1:g.100193T>A , LRG_47:g.100193T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000470918.2:n.4614T>A
ENST00000695970.1:c.3412T>A ENSP00000512297.1:p.Ser1138Thr
ENST00000695971.1:c.3565T>A ENSP00000512298.1:p.Ser1189Thr
ENST00000695972.1:c.*663T>A ENSP00000512299.1:n.*663T>A
ENST00000695973.1:c.*1950T>A ENSP00000512300.1:n.*1950T>A
ENST00000695974.1:c.3409T>A ENSP00000512301.1:p.Ser1137Thr
ENST00000695975.1:c.*1713T>A ENSP00000512302.1:n.*1713T>A
ENST00000695976.1:c.3397T>A ENSP00000512303.1:p.Ser1133Thr
ENST00000695981.1:c.3580+6T>A ENSP00000512306.1:n.3580+6T>A
ENST00000695984.1:c.1594T>A ENSP00000512309.1:p.Ser532Thr
ENST00000695986.1:c.*3237T>A ENSP00000512311.1:n.*3237T>A
ENST00000695990.1:n.620T>A
ENST00000696026.1:c.*1868T>A ENSP00000512335.1:n.*1868T>A
ENST00000696027.1:c.3580T>A ENSP00000512336.1:p.Ser1194Thr
ENST00000696028.1:c.3514T>A ENSP00000512337.1:p.Ser1172Thr
ENST00000696029.1:c.3580T>A ENSP00000512338.1:p.Ser1194Thr
ENST00000696031.1:c.*3104T>A ENSP00000512340.1:n.*3104T>A
ENST00000696032.1:c.3580+6T>A ENSP00000512341.1:n.3580+6T>A
ENST00000696033.1:c.1160-32594T>A ENSP00000512342.1:n.1160-32594T>A
ENST00000367429.9:c.3586T>A MANE Select ENSP00000356399.4:p.Ser1196Thr
ENST00000367429.8:c.3586T>A ENSP00000356399.4:p.Ser1196Thr
ENST00000466229.5:n.6684T>A
NM_000186.3:c.3586T>A , LRG_47t1:c.3586T>A NP_000177.2:p.Ser1196Thr
XR_001737134.2:n.3772T>A
NM_000186.4:c.3586T>A MANE Select NP_000177.2:p.Ser1196Thr