Human (GRCh38.p14)
Description

complement factor B [Source:HGNC Symbol;Acc:HGNC:1037]

Gene Synonyms

BF, BFD, H2-BF

Location

Scaffold HSCHR6_MHC_MANN_CTG1: 3,250,627-3,255,741 forward strand.

GRCh38:GL000253.2

View this gene on the primary assembly.

About this gene

This gene has 10 transcripts (splice variants), 1 gene allele and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000375455.7CFB-2021996589aaENSP00000364604.3
 
Protein coding
A0A0G2JH38 -Ensembl CanonicalGENCODE basicTSL:1CDS 3' incomplete
ENST00000375443.3CFB-2011921589aaENSP00000364592.3
 
Protein coding
A0A0G2JH38 -TSL:5CDS 3' incomplete
ENST00000489605.5CFB-209743No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000463942.5CFB-204736No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000498489.5CFB-210568No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000477842.5CFB-2051866No protein-
 
Retained intron
--TSL:2
ENST00000487158.5CFB-2071277No protein-
 
Retained intron
--TSL:5
ENST00000479302.1CFB-206896No protein-
 
Retained intron
--TSL:3
ENST00000461569.1CFB-203685No protein-
 
Retained intron
--TSL:2
ENST00000487765.1CFB-208526No protein-
 
Retained intron
--TSL:2