Canonical Allele Identifier: CA2649647281

Gene: CFH

Linked Data

• gnomAD v4: 1-196747368-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747368C>G , CM000663.2:g.196747368C>G	GRCh38
NC_000001.10:g.196716498C>G , CM000663.1:g.196716498C>G	GRCh37
NC_000001.9:g.194983121C>G	NCBI36
NG_007259.1:g.100358C>G , LRG_47:g.100358C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4779C>G
ENST00000695970.1:c.*55C>G	ENSP00000512297.1:n.*55C>G
ENST00000695971.1:c.*55C>G	ENSP00000512298.1:n.*55C>G
ENST00000695972.1:c.*828C>G	ENSP00000512299.1:n.*828C>G
ENST00000695973.1:c.*2115C>G	ENSP00000512300.1:n.*2115C>G
ENST00000695974.1:c.*55C>G	ENSP00000512301.1:n.*55C>G
ENST00000695975.1:c.*1878C>G	ENSP00000512302.1:n.*1878C>G
ENST00000695976.1:c.*55C>G	ENSP00000512303.1:n.*55C>G
ENST00000695981.1:c.3580+171C>G	ENSP00000512306.1:n.3580+171C>G
ENST00000695984.1:c.*55C>G	ENSP00000512309.1:n.*55C>G
ENST00000695986.1:c.*3402C>G	ENSP00000512311.1:n.*3402C>G
ENST00000695990.1:n.785C>G
ENST00000696026.1:c.*2033C>G	ENSP00000512335.1:n.*2033C>G
ENST00000696027.1:c.*55C>G	ENSP00000512336.1:n.*55C>G
ENST00000696028.1:c.*55C>G	ENSP00000512337.1:n.*55C>G
ENST00000696029.1:c.*55C>G	ENSP00000512338.1:n.*55C>G
ENST00000696031.1:c.*3269C>G	ENSP00000512340.1:n.*3269C>G
ENST00000696032.1:c.3580+171C>G	ENSP00000512341.1:n.3580+171C>G
ENST00000696033.1:c.1160-32429C>G	ENSP00000512342.1:n.1160-32429C>G
ENST00000367429.9:c.*55C>G MANE Select	ENSP00000356399.4:n.*55C>G
ENST00000367429.8:c.*55C>G	ENSP00000356399.4:n.*55C>G
ENST00000466229.5:n.6849C>G
NM_000186.3:c.*55C>G , LRG_47t1:c.*55C>G	NP_000177.2:n.*55C>G
XR_001737134.2:n.3937C>G
NM_000186.4:c.*55C>G MANE Select	NP_000177.2:n.*55C>G