Canonical Allele Identifier: CA343983728

Gene: CFH

Linked Data

• MyVariant Identifiers: chr1:g.196712689T>C (hg19) ; chr1:g.196743559T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196743559T>C , CM000663.2:g.196743559T>C	GRCh38
NC_000001.10:g.196712689T>C , CM000663.1:g.196712689T>C	GRCh37
NC_000001.9:g.194979312T>C	NCBI36
NG_007259.1:g.96549T>C , LRG_47:g.96549T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470918.2:n.4269T>C
ENST00000695970.1:c.3067T>C	ENSP00000512297.1:p.Tyr1023His
ENST00000695971.1:c.3220T>C	ENSP00000512298.1:p.Tyr1074His
ENST00000695972.1:c.*318T>C	ENSP00000512299.1:n.*318T>C
ENST00000695973.1:c.*1605T>C	ENSP00000512300.1:n.*1605T>C
ENST00000695974.1:c.3064T>C	ENSP00000512301.1:p.Tyr1022His
ENST00000695975.1:c.*1368T>C	ENSP00000512302.1:n.*1368T>C
ENST00000695976.1:c.3052T>C	ENSP00000512303.1:p.Tyr1018His
ENST00000695981.1:c.3241T>C	ENSP00000512306.1:p.Tyr1081His
ENST00000695984.1:c.1249T>C	ENSP00000512309.1:p.Tyr417His
ENST00000695986.1:c.*2892T>C	ENSP00000512311.1:n.*2892T>C
ENST00000696026.1:c.*1523T>C	ENSP00000512335.1:n.*1523T>C
ENST00000696027.1:c.3235T>C	ENSP00000512336.1:p.Tyr1079His
ENST00000696028.1:c.3169T>C	ENSP00000512337.1:p.Tyr1057His
ENST00000696029.1:c.3235T>C	ENSP00000512338.1:p.Tyr1079His
ENST00000696031.1:c.*2759T>C	ENSP00000512340.1:n.*2759T>C
ENST00000696032.1:c.3241T>C	ENSP00000512341.1:p.Tyr1081His
ENST00000696033.1:c.1160-36238T>C	ENSP00000512342.1:n.1160-36238T>C
ENST00000367429.9:c.3241T>C MANE Select	ENSP00000356399.4:p.Tyr1081His
ENST00000367429.8:c.3241T>C	ENSP00000356399.4:p.Tyr1081His
ENST00000466229.5:n.6339T>C
NM_000186.3:c.3241T>C , LRG_47t1:c.3241T>C	NP_000177.2:p.Tyr1081His
XR_001737134.2:n.3427T>C
NM_000186.4:c.3241T>C MANE Select	NP_000177.2:p.Tyr1081His