Canonical Allele Identifier: CA1619378418
Gene: CFB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31950521A= , CM000668.2:g.31950521A= GRCh38
NC_000006.11:g.31918298A= , CM000668.1:g.31918298A= GRCh37
NC_000006.10:g.32026277A= NCBI36
NG_008191.1:g.9578A= , LRG_136:g.9578A=

Transcript Alleles

HGVS Amino-acid change
ENST00000452035.7:n.1919A=
ENST00000483004.2:c.1409-98A= ENSP00000419887.2:n.1409-98A=
ENST00000698628.1:c.1624+118A= ENSP00000513848.1:n.1624+118A=
ENST00000698629.1:n.1802-98A=
ENST00000698630.1:n.2341-98A=
ENST00000698631.1:n.2342-98A=
ENST00000698632.1:n.3038A=
ENST00000698633.1:n.2928A=
ENST00000698636.1:n.1847-98A=
ENST00000425368.7:c.1625-98A= MANE Select ENSP00000416561.2:n.1625-98A=
ENST00000425368.6:c.1625-98A= ENSP00000416561.2:n.1625-98A=
ENST00000452035.6:n.1742A=
ENST00000456570.5:c.3131-98A= ENSP00000410815.1:n.3131-98A=
ENST00000467360.1:n.653A=
ENST00000477310.1:c.2678-98A= ENSP00000418996.1:n.2678-98A=
ENST00000483004.1:c.247-98A=
NM_001710.5:c.1625-98A= , LRG_136t1:c.1625-98A= NP_001701.2:n.1625-98A=
NM_001710.6:c.1625-98A= MANE Select NP_001701.2:n.1625-98A=