Canonical Allele Identifier: CA1619378312
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31950401T= , CM000668.2:g.31950401T= GRCh38
NC_000006.11:g.31918178T= , CM000668.1:g.31918178T= GRCh37
NC_000006.10:g.32026157T= NCBI36
NG_008191.1:g.9458T= , LRG_136:g.9458T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452035.7:n.1799T=
ENST00000483004.2:c.1409-218T= ENSP00000419887.2:n.1409-218T=
ENST00000698628.1:c.1622T= ENSP00000513848.1:p.Val541=
ENST00000698629.1:n.1799T=
ENST00000698630.1:n.2338T=
ENST00000698631.1:n.2339T=
ENST00000698632.1:n.2918T=
ENST00000698633.1:n.2808T=
ENST00000698636.1:n.1844T=
ENST00000425368.7:c.1622T= MANE Select ENSP00000416561.2:p.Val541=
ENST00000425368.6:c.1622T= ENSP00000416561.2:p.Val541=
ENST00000452035.6:n.1622T=
ENST00000456570.5:c.3128T= ENSP00000410815.1:p.Val1043=
ENST00000467360.1:n.533T=
ENST00000477310.1:c.2675T= ENSP00000418996.1:p.Val892=
ENST00000483004.1:c.247-218T=
NM_001710.5:c.1622T= , LRG_136t1:c.1622T= NP_001701.2:p.Val541=
NM_001710.6:c.1622T= MANE Select NP_001701.2:p.Val541=