Canonical Allele Identifier: CA729697591

Gene: CFH

Linked Data

• dbSNP Id: rs1442944081
• gnomAD v4: 1-196747360-T-A
• MyVariant Identifiers: chr1:g.196716490T>A (hg19) ; chr1:g.196747360T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196747360T>A , CM000663.2:g.196747360T>A	GRCh38
NC_000001.10:g.196716490T>A , CM000663.1:g.196716490T>A	GRCh37
NC_000001.9:g.194983113T>A	NCBI36
NG_007259.1:g.100350T>A , LRG_47:g.100350T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.4771T>A
ENST00000695970.1:c.*47T>A	ENSP00000512297.1:n.*47T>A
ENST00000695971.1:c.*47T>A	ENSP00000512298.1:n.*47T>A
ENST00000695972.1:c.*820T>A	ENSP00000512299.1:n.*820T>A
ENST00000695973.1:c.*2107T>A	ENSP00000512300.1:n.*2107T>A
ENST00000695974.1:c.*47T>A	ENSP00000512301.1:n.*47T>A
ENST00000695975.1:c.*1870T>A	ENSP00000512302.1:n.*1870T>A
ENST00000695976.1:c.*47T>A	ENSP00000512303.1:n.*47T>A
ENST00000695981.1:c.3580+163T>A	ENSP00000512306.1:n.3580+163T>A
ENST00000695984.1:c.*47T>A	ENSP00000512309.1:n.*47T>A
ENST00000695986.1:c.*3394T>A	ENSP00000512311.1:n.*3394T>A
ENST00000695990.1:n.777T>A
ENST00000696026.1:c.*2025T>A	ENSP00000512335.1:n.*2025T>A
ENST00000696027.1:c.*47T>A	ENSP00000512336.1:n.*47T>A
ENST00000696028.1:c.*47T>A	ENSP00000512337.1:n.*47T>A
ENST00000696029.1:c.*47T>A	ENSP00000512338.1:n.*47T>A
ENST00000696031.1:c.*3261T>A	ENSP00000512340.1:n.*3261T>A
ENST00000696032.1:c.3580+163T>A	ENSP00000512341.1:n.3580+163T>A
ENST00000696033.1:c.1160-32437T>A	ENSP00000512342.1:n.1160-32437T>A
ENST00000367429.9:c.*47T>A MANE Select	ENSP00000356399.4:n.*47T>A
ENST00000367429.8:c.*47T>A	ENSP00000356399.4:n.*47T>A
ENST00000466229.5:n.6841T>A
NM_000186.3:c.*47T>A , LRG_47t1:c.*47T>A	NP_000177.2:n.*47T>A
XR_001737134.2:n.3929T>A
NM_000186.4:c.*47T>A MANE Select	NP_000177.2:n.*47T>A