Canonical Allele Identifier: CA422663418

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196716242T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747112T>C , CM000663.2:g.196747112T>C	GRCh38
NC_000001.10:g.196716242T>C , CM000663.1:g.196716242T>C	GRCh37
NC_000001.9:g.194982865T>C	NCBI36
NG_007259.1:g.100102T>C , LRG_47:g.100102T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4523T>C
ENST00000695970.1:c.3321T>C	ENSP00000512297.1:p.His1107=
ENST00000695971.1:c.3474T>C	ENSP00000512298.1:p.His1158=
ENST00000695972.1:c.*572T>C	ENSP00000512299.1:n.*572T>C
ENST00000695973.1:c.*1859T>C	ENSP00000512300.1:n.*1859T>C
ENST00000695974.1:c.3318T>C	ENSP00000512301.1:p.His1106=
ENST00000695975.1:c.*1622T>C	ENSP00000512302.1:n.*1622T>C
ENST00000695976.1:c.3306T>C	ENSP00000512303.1:p.His1102=
ENST00000695981.1:c.3495T>C	ENSP00000512306.1:p.His1165=
ENST00000695984.1:c.1503T>C	ENSP00000512309.1:p.His501=
ENST00000695986.1:c.*3146T>C	ENSP00000512311.1:n.*3146T>C
ENST00000695990.1:n.529T>C
ENST00000696026.1:c.*1777T>C	ENSP00000512335.1:n.*1777T>C
ENST00000696027.1:c.3489T>C	ENSP00000512336.1:p.His1163=
ENST00000696028.1:c.3423T>C	ENSP00000512337.1:p.His1141=
ENST00000696029.1:c.3489T>C	ENSP00000512338.1:p.His1163=
ENST00000696031.1:c.*3013T>C	ENSP00000512340.1:n.*3013T>C
ENST00000696032.1:c.3495T>C	ENSP00000512341.1:p.His1165=
ENST00000696033.1:c.1160-32685T>C	ENSP00000512342.1:n.1160-32685T>C
ENST00000367429.9:c.3495T>C MANE Select	ENSP00000356399.4:p.His1165=
ENST00000367429.8:c.3495T>C	ENSP00000356399.4:p.His1165=
ENST00000466229.5:n.6593T>C
NM_000186.3:c.3495T>C , LRG_47t1:c.3495T>C	NP_000177.2:p.His1165=
XR_001737134.2:n.3681T>C
NM_000186.4:c.3495T>C MANE Select	NP_000177.2:p.His1165=