Canonical Allele Identifier: CA343989199
Gene: CFH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196747277T>A , CM000663.2:g.196747277T>A GRCh38
NC_000001.10:g.196716407T>A , CM000663.1:g.196716407T>A GRCh37
NC_000001.9:g.194983030T>A NCBI36
NG_007259.1:g.100267T>A , LRG_47:g.100267T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367429.9:c.3660T>A MANE Select ENSP00000356399.4:p.Asp1220Glu
ENST00000367429.8:c.3660T>A ENSP00000356399.4:p.Asp1220Glu
ENST00000466229.5:n.6758T>A
NM_000186.3:c.3660T>A , LRG_47t1:c.3660T>A NP_000177.2:p.Asp1220Glu
XR_001737134.2:n.3846T>A
NM_000186.4:c.3660T>A MANE Select NP_000177.2:p.Asp1220Glu