Canonical Allele Identifier: CA1619374723
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31946406C= , CM000668.2:g.31946406C= GRCh38
NC_000006.11:g.31914183C= , CM000668.1:g.31914183C= GRCh37
NC_000006.10:g.32022162C= NCBI36
NG_008191.1:g.5463C= , LRG_136:g.5463C=
NG_011730.1:g.23918C= , LRG_26:g.23918C=

Transcript Alleles

HGVS Amino-acid change
ENST00000452035.7:n.275C=
ENST00000483004.2:c.98C= ENSP00000419887.2:p.Pro33=
ENST00000497841.6:c.98C= ENSP00000513847.1:p.Pro33=
ENST00000698628.1:c.98C= ENSP00000513848.1:p.Pro33=
ENST00000698629.1:n.275C=
ENST00000698630.1:n.259C=
ENST00000698631.1:n.254C=
ENST00000698632.1:n.226C=
ENST00000698633.1:n.196C=
ENST00000698636.1:n.320C=
ENST00000425368.7:c.98C= MANE Select ENSP00000416561.2:p.Pro33=
ENST00000425368.6:c.98C= ENSP00000416561.2:p.Pro33=
ENST00000452035.6:n.98C=
ENST00000456570.5:c.1604C= ENSP00000410815.1:p.Pro535=
ENST00000460718.5:c.65-80C= ENSP00000417793.1:n.65-80C=
ENST00000472581.1:n.345C=
ENST00000475617.5:c.98C= ENSP00000420090.1:p.Pro33=
ENST00000477310.1:c.1352-601C= ENSP00000418996.1:n.1352-601C=
NM_001710.5:c.98C= , LRG_136t1:c.98C= NP_001701.2:p.Pro33=
NM_001710.6:c.98C= MANE Select NP_001701.2:p.Pro33=