Canonical Allele Identifier: CA343982077

Gene: CFH

Linked Data

• ClinVar Variation Id: 2805595
• ClinVar RCV Id: RCV003676842
• MyVariant Identifiers: chr1:g.196682972G>T (hg19) ; chr1:g.196713842G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196713842G>T , CM000663.2:g.196713842G>T	GRCh38
NC_000001.10:g.196682972G>T , CM000663.1:g.196682972G>T	GRCh37
NC_000001.9:g.194949595G>T	NCBI36
NG_007259.1:g.66832G>T , LRG_47:g.66832G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470918.2:n.1710G>T
ENST00000695969.1:c.1444G>T	ENSP00000512296.1:p.Val482Leu
ENST00000695970.1:c.1444G>T	ENSP00000512297.1:p.Val482Leu
ENST00000695971.1:c.1423G>T	ENSP00000512298.1:p.Val475Leu
ENST00000695972.1:c.1444G>T	ENSP00000512299.1:p.Val482Leu
ENST00000695973.1:c.1444G>T	ENSP00000512300.1:p.Val482Leu
ENST00000695974.1:c.1444G>T	ENSP00000512301.1:p.Val482Leu
ENST00000695975.1:c.1444G>T	ENSP00000512302.1:p.Val482Leu
ENST00000695976.1:c.1255G>T	ENSP00000512303.1:p.Val419Leu
ENST00000695981.1:c.1444G>T	ENSP00000512306.1:p.Val482Leu
ENST00000695983.1:c.1444G>T	ENSP00000512308.1:p.Val482Leu
ENST00000695984.1:c.245-14504G>T	ENSP00000512309.1:n.245-14504G>T
ENST00000695986.1:c.*1095G>T	ENSP00000512311.1:n.*1095G>T
ENST00000696024.1:n.1528G>T
ENST00000696025.1:n.1528G>T
ENST00000696026.1:c.1444G>T	ENSP00000512335.1:p.Val482Leu
ENST00000696027.1:c.1444G>T	ENSP00000512336.1:p.Val482Leu
ENST00000696028.1:c.1444G>T	ENSP00000512337.1:p.Val482Leu
ENST00000696029.1:c.1444G>T	ENSP00000512338.1:p.Val482Leu
ENST00000696031.1:c.*962G>T	ENSP00000512340.1:n.*962G>T
ENST00000696032.1:c.1444G>T	ENSP00000512341.1:p.Val482Leu
ENST00000696033.1:c.1159+24228G>T	ENSP00000512342.1:n.1159+24228G>T
ENST00000367429.9:c.1444G>T MANE Select	ENSP00000356399.4:p.Val482Leu
ENST00000367429.8:c.1444G>T	ENSP00000356399.4:p.Val482Leu
ENST00000466229.5:n.3460G>T
NM_000186.3:c.1444G>T , LRG_47t1:c.1444G>T	NP_000177.2:p.Val482Leu
XR_001737134.2:n.1529G>T
NM_000186.4:c.1444G>T MANE Select	NP_000177.2:p.Val482Leu