Canonical Allele Identifier: CA343983594

Gene: CFH

Linked Data

• dbSNP Id: rs750509800
• gnomAD v2: 1-196712672-A-G
• gnomAD v4: 1-196743542-A-G
• MyVariant Identifiers: chr1:g.196712672A>G (hg19) ; chr1:g.196743542A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743542A>G , CM000663.2:g.196743542A>G	GRCh38
NC_000001.10:g.196712672A>G , CM000663.1:g.196712672A>G	GRCh37
NC_000001.9:g.194979295A>G	NCBI36
NG_007259.1:g.96532A>G , LRG_47:g.96532A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4252A>G
ENST00000695970.1:c.3050A>G	ENSP00000512297.1:p.Tyr1017Cys
ENST00000695971.1:c.3203A>G	ENSP00000512298.1:p.Tyr1068Cys
ENST00000695972.1:c.*301A>G	ENSP00000512299.1:n.*301A>G
ENST00000695973.1:c.*1588A>G	ENSP00000512300.1:n.*1588A>G
ENST00000695974.1:c.3047A>G	ENSP00000512301.1:p.Tyr1016Cys
ENST00000695975.1:c.*1351A>G	ENSP00000512302.1:n.*1351A>G
ENST00000695976.1:c.3035A>G	ENSP00000512303.1:p.Tyr1012Cys
ENST00000695981.1:c.3224A>G	ENSP00000512306.1:p.Tyr1075Cys
ENST00000695984.1:c.1232A>G	ENSP00000512309.1:p.Tyr411Cys
ENST00000695986.1:c.*2875A>G	ENSP00000512311.1:n.*2875A>G
ENST00000696026.1:c.*1506A>G	ENSP00000512335.1:n.*1506A>G
ENST00000696027.1:c.3218A>G	ENSP00000512336.1:p.Tyr1073Cys
ENST00000696028.1:c.3152A>G	ENSP00000512337.1:p.Tyr1051Cys
ENST00000696029.1:c.3218A>G	ENSP00000512338.1:p.Tyr1073Cys
ENST00000696031.1:c.*2742A>G	ENSP00000512340.1:n.*2742A>G
ENST00000696032.1:c.3224A>G	ENSP00000512341.1:p.Tyr1075Cys
ENST00000696033.1:c.1160-36255A>G	ENSP00000512342.1:n.1160-36255A>G
ENST00000367429.9:c.3224A>G MANE Select	ENSP00000356399.4:p.Tyr1075Cys
ENST00000367429.8:c.3224A>G	ENSP00000356399.4:p.Tyr1075Cys
ENST00000466229.5:n.6322A>G
NM_000186.3:c.3224A>G , LRG_47t1:c.3224A>G	NP_000177.2:p.Tyr1075Cys
XR_001737134.2:n.3410A>G
NM_000186.4:c.3224A>G MANE Select	NP_000177.2:p.Tyr1075Cys