Canonical Allele Identifier: CA1619378510
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31950639G= , CM000668.2:g.31950639G= GRCh38
NC_000006.11:g.31918416G= , CM000668.1:g.31918416G= GRCh37
NC_000006.10:g.32026395G= NCBI36
NG_008191.1:g.9696G= , LRG_136:g.9696G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000452035.7:n.2037G=
ENST00000483004.2:c.1429G= ENSP00000419887.2:p.Glu477=
ENST00000698628.1:c.1624+236G= ENSP00000513848.1:n.1624+236G=
ENST00000698629.1:n.1822G=
ENST00000698630.1:n.2361G=
ENST00000698631.1:n.2362G=
ENST00000698632.1:n.3156G=
ENST00000698633.1:n.3046G=
ENST00000698636.1:n.1867G=
ENST00000425368.7:c.1645G= MANE Select ENSP00000416561.2:p.Glu549=
ENST00000425368.6:c.1645G= ENSP00000416561.2:p.Glu549=
ENST00000452035.6:n.1860G=
ENST00000456570.5:c.3151G= ENSP00000410815.1:p.Glu1051=
ENST00000467360.1:n.771G=
ENST00000477310.1:c.2698G= ENSP00000418996.1:p.Glu900=
ENST00000483004.1:c.267G=
NM_001710.5:c.1645G= , LRG_136t1:c.1645G= NP_001701.2:p.Glu549=
NM_001710.6:c.1645G= MANE Select NP_001701.2:p.Glu549=