Canonical Allele Identifier: CA343989176
Gene: CFH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196747274G>C , CM000663.2:g.196747274G>C GRCh38
NC_000001.10:g.196716404G>C , CM000663.1:g.196716404G>C GRCh37
NC_000001.9:g.194983027G>C NCBI36
NG_007259.1:g.100264G>C , LRG_47:g.100264G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367429.9:c.3657G>C MANE Select ENSP00000356399.4:p.Trp1219Cys
ENST00000367429.8:c.3657G>C ENSP00000356399.4:p.Trp1219Cys
NM_000186.3:c.3657G>C , LRG_47t1:c.3657G>C NP_000177.2:p.Trp1219Cys
NM_000186.4:c.3657G>C MANE Select NP_000177.2:p.Trp1219Cys