Canonical Allele Identifier: CA422663596

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196716365T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747235T>C , CM000663.2:g.196747235T>C	GRCh38
NC_000001.10:g.196716365T>C , CM000663.1:g.196716365T>C	GRCh37
NC_000001.9:g.194982988T>C	NCBI36
NG_007259.1:g.100225T>C , LRG_47:g.100225T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4646T>C
ENST00000695970.1:c.3444T>C	ENSP00000512297.1:p.Arg1148=
ENST00000695971.1:c.3597T>C	ENSP00000512298.1:p.Arg1199=
ENST00000695972.1:c.*695T>C	ENSP00000512299.1:n.*695T>C
ENST00000695973.1:c.*1982T>C	ENSP00000512300.1:n.*1982T>C
ENST00000695974.1:c.3441T>C	ENSP00000512301.1:p.Arg1147=
ENST00000695975.1:c.*1745T>C	ENSP00000512302.1:n.*1745T>C
ENST00000695976.1:c.3429T>C	ENSP00000512303.1:p.Arg1143=
ENST00000695981.1:c.3580+38T>C	ENSP00000512306.1:n.3580+38T>C
ENST00000695984.1:c.1626T>C	ENSP00000512309.1:p.Arg542=
ENST00000695986.1:c.*3269T>C	ENSP00000512311.1:n.*3269T>C
ENST00000695990.1:n.652T>C
ENST00000696026.1:c.*1900T>C	ENSP00000512335.1:n.*1900T>C
ENST00000696027.1:c.3612T>C	ENSP00000512336.1:p.Arg1204=
ENST00000696028.1:c.3546T>C	ENSP00000512337.1:p.Arg1182=
ENST00000696029.1:c.3612T>C	ENSP00000512338.1:p.Arg1204=
ENST00000696031.1:c.*3136T>C	ENSP00000512340.1:n.*3136T>C
ENST00000696032.1:c.3580+38T>C	ENSP00000512341.1:n.3580+38T>C
ENST00000696033.1:c.1160-32562T>C	ENSP00000512342.1:n.1160-32562T>C
ENST00000367429.9:c.3618T>C MANE Select	ENSP00000356399.4:p.Arg1206=
ENST00000367429.8:c.3618T>C	ENSP00000356399.4:p.Arg1206=
ENST00000466229.5:n.6716T>C
NM_000186.3:c.3618T>C , LRG_47t1:c.3618T>C	NP_000177.2:p.Arg1206=
XR_001737134.2:n.3804T>C
NM_000186.4:c.3618T>C MANE Select	NP_000177.2:p.Arg1206=