Human (GRCh38.p14)
Description

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

Gene Synonyms

BF, BFD, H2-BF

Location

Scaffold HSCHR6_MHC_DBB_CTG1: 3,193,430-3,199,864 forward strand.

GRCh38:GL000252.2

View this gene on the primary assembly.

About this gene

This gene has 12 transcripts (splice variants), 1 gene allele and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000433503.2CFB-2352577764aaENSP00000388352.2
 
Protein coding
P00751-1 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000455591.5CFB-2362502764aaENSP00000414341.1
 
Protein coding
P00751-1 -GENCODE basicTSL:5
ENST00000474621.5CFB-239743No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000487665.5CFB-244736No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000469094.5CFB-238568No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000477655.5CFB-2421866No protein-
 
Retained intron
--TSL:2
ENST00000475203.5CFB-2401277No protein-
 
Retained intron
--TSL:5
ENST00000481375.1CFB-2431082No protein-
 
Retained intron
--TSL:5
ENST00000494916.1CFB-246764No protein-
 
Retained intron
--TSL:2
ENST00000494049.1CFB-245685No protein-
 
Retained intron
--TSL:2
ENST00000476879.1CFB-241589No protein-
 
Retained intron
--TSL:2
ENST00000465106.1CFB-237526No protein-
 
Retained intron
--TSL:2