Canonical Allele Identifier: CA343984109

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196712749C>T (hg19) ; chr1:g.196743619C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743619C>T , CM000663.2:g.196743619C>T	GRCh38
NC_000001.10:g.196712749C>T , CM000663.1:g.196712749C>T	GRCh37
NC_000001.9:g.194979372C>T	NCBI36
NG_007259.1:g.96609C>T , LRG_47:g.96609C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4329C>T
ENST00000695970.1:c.3127C>T	ENSP00000512297.1:p.Gln1043Ter
ENST00000695971.1:c.3280C>T	ENSP00000512298.1:p.Gln1094Ter
ENST00000695972.1:c.*378C>T	ENSP00000512299.1:n.*378C>T
ENST00000695973.1:c.*1665C>T	ENSP00000512300.1:n.*1665C>T
ENST00000695974.1:c.3124C>T	ENSP00000512301.1:p.Gln1042Ter
ENST00000695975.1:c.*1428C>T	ENSP00000512302.1:n.*1428C>T
ENST00000695976.1:c.3112C>T	ENSP00000512303.1:p.Gln1038Ter
ENST00000695981.1:c.3301C>T	ENSP00000512306.1:p.Gln1101Ter
ENST00000695984.1:c.1309C>T	ENSP00000512309.1:p.Gln437Ter
ENST00000695986.1:c.*2952C>T	ENSP00000512311.1:n.*2952C>T
ENST00000696026.1:c.*1583C>T	ENSP00000512335.1:n.*1583C>T
ENST00000696027.1:c.3295C>T	ENSP00000512336.1:p.Gln1099Ter
ENST00000696028.1:c.3229C>T	ENSP00000512337.1:p.Gln1077Ter
ENST00000696029.1:c.3295C>T	ENSP00000512338.1:p.Gln1099Ter
ENST00000696031.1:c.*2819C>T	ENSP00000512340.1:n.*2819C>T
ENST00000696032.1:c.3301C>T	ENSP00000512341.1:p.Gln1101Ter
ENST00000696033.1:c.1160-36178C>T	ENSP00000512342.1:n.1160-36178C>T
ENST00000367429.9:c.3301C>T MANE Select	ENSP00000356399.4:p.Gln1101Ter
ENST00000367429.8:c.3301C>T	ENSP00000356399.4:p.Gln1101Ter
ENST00000466229.5:n.6399C>T
NM_000186.3:c.3301C>T , LRG_47t1:c.3301C>T	NP_000177.2:p.Gln1101Ter
XR_001737134.2:n.3487C>T
NM_000186.4:c.3301C>T MANE Select	NP_000177.2:p.Gln1101Ter