Canonical Allele Identifier: CA10747848
Gene: CFH HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2284664

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196733395C>T , CM000663.2:g.196733395C>T GRCh38
NC_000001.10:g.196702525C>T , CM000663.1:g.196702525C>T GRCh37
NC_000001.9:g.194969148C>T NCBI36
NG_007259.1:g.86385C>T , LRG_47:g.86385C>T

Transcript Alleles

HGVS Amino-acid change
NM_000186.3:c.2414-3429C>T , LRG_47t1:c.2414-3429C>T NP_000177.2:p.=
XR_001737134.2:n.2600-3429C>T
ENST00000367429.8:c.2414-3429C>T ENSP00000356399.4:p.=
ENST00000466229.5:n.4430-3429C>T