Canonical Allele Identifier: CA343983768

Gene: CFH

Linked Data

• dbSNP Id: rs1356969065
• gnomAD v2: 1-196684892-A-G
• gnomAD v4: 1-196715762-A-G
• MyVariant Identifiers: chr1:g.196684892A>G (hg19) ; chr1:g.196715762A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196715762A>G , CM000663.2:g.196715762A>G	GRCh38
NC_000001.10:g.196684892A>G , CM000663.1:g.196684892A>G	GRCh37
NC_000001.9:g.194951515A>G	NCBI36
NG_007259.1:g.68752A>G , LRG_47:g.68752A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.1955A>G
ENST00000695969.1:c.1689A>G	ENSP00000512296.1:p.Ile563Met
ENST00000695970.1:c.1689A>G	ENSP00000512297.1:p.Ile563Met
ENST00000695971.1:c.1668A>G	ENSP00000512298.1:p.Ile556Met
ENST00000695972.1:c.1689A>G	ENSP00000512299.1:p.Ile563Met
ENST00000695973.1:c.1689A>G	ENSP00000512300.1:p.Ile563Met
ENST00000695974.1:c.1689A>G	ENSP00000512301.1:p.Ile563Met
ENST00000695975.1:c.1689A>G	ENSP00000512302.1:p.Ile563Met
ENST00000695976.1:c.1500A>G	ENSP00000512303.1:p.Ile500Met
ENST00000695981.1:c.1689A>G	ENSP00000512306.1:p.Ile563Met
ENST00000695983.1:c.1689A>G	ENSP00000512308.1:p.Ile563Met
ENST00000695984.1:c.245-12584A>G	ENSP00000512309.1:n.245-12584A>G
ENST00000695986.1:c.*1340A>G	ENSP00000512311.1:n.*1340A>G
ENST00000696024.1:n.1773A>G
ENST00000696025.1:n.1773A>G
ENST00000696026.1:c.1689A>G	ENSP00000512335.1:p.Ile563Met
ENST00000696027.1:c.1689A>G	ENSP00000512336.1:p.Ile563Met
ENST00000696028.1:c.1689A>G	ENSP00000512337.1:p.Ile563Met
ENST00000696029.1:c.1689A>G	ENSP00000512338.1:p.Ile563Met
ENST00000696031.1:c.*1207A>G	ENSP00000512340.1:n.*1207A>G
ENST00000696032.1:c.1689A>G	ENSP00000512341.1:p.Ile563Met
ENST00000696033.1:c.1159+26148A>G	ENSP00000512342.1:n.1159+26148A>G
ENST00000367429.9:c.1689A>G MANE Select	ENSP00000356399.4:p.Ile563Met
ENST00000367429.8:c.1689A>G	ENSP00000356399.4:p.Ile563Met
ENST00000466229.5:n.3705A>G
NM_000186.3:c.1689A>G , LRG_47t1:c.1689A>G	NP_000177.2:p.Ile563Met
XR_001737134.2:n.1774A>G
NM_000186.4:c.1689A>G MANE Select	NP_000177.2:p.Ile563Met