Canonical Allele Identifier: CA1619374725
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31946407C= , CM000668.2:g.31946407C= GRCh38
NC_000006.11:g.31914184C= , CM000668.1:g.31914184C= GRCh37
NC_000006.10:g.32022163C= NCBI36
NG_008191.1:g.5464C= , LRG_136:g.5464C=
NG_011730.1:g.23919C= , LRG_26:g.23919C=

Transcript Alleles

HGVS Amino-acid change
ENST00000452035.7:n.276C=
ENST00000483004.2:c.99C= ENSP00000419887.2:p.Pro33=
ENST00000497841.6:c.99C= ENSP00000513847.1:p.Pro33=
ENST00000698628.1:c.99C= ENSP00000513848.1:p.Pro33=
ENST00000698629.1:n.276C=
ENST00000698630.1:n.260C=
ENST00000698631.1:n.255C=
ENST00000698632.1:n.227C=
ENST00000698633.1:n.197C=
ENST00000698636.1:n.321C=
ENST00000425368.7:c.99C= MANE Select ENSP00000416561.2:p.Pro33=
ENST00000425368.6:c.99C= ENSP00000416561.2:p.Pro33=
ENST00000452035.6:n.99C=
ENST00000456570.5:c.1605C= ENSP00000410815.1:p.Pro535=
ENST00000460718.5:c.65-79C= ENSP00000417793.1:n.65-79C=
ENST00000472581.1:n.346C=
ENST00000475617.5:c.99C= ENSP00000420090.1:p.Pro33=
ENST00000477310.1:c.1352-600C= ENSP00000418996.1:n.1352-600C=
NM_001710.5:c.99C= , LRG_136t1:c.99C= NP_001701.2:p.Pro33=
NM_001710.6:c.99C= MANE Select NP_001701.2:p.Pro33=