Human (GRCh38.p14)
Description

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

Gene Synonyms

BF, BFD, H2-BF

Location

Scaffold HSCHR6_MHC_MCF_CTG1: 3,287,686-3,294,120 forward strand.

GRCh38:GL000254.2

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
ENST00000436692.2CFB-2602577764aaENSP00000389604.2
 
Protein coding
P00751-1 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000424727.5CFB-2592502764aaENSP00000401719.1
 
Protein coding
P00751-1 -GENCODE basicTSL:5
ENST00000473139.5CFB-264743No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000498577.5CFB-270736No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000482919.5CFB-267568No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000481722.5CFB-2661866No protein-
 
Retained intron
--TSL:2
ENST00000472676.5CFB-2631277No protein-
 
Retained intron
--TSL:5
ENST00000484102.1CFB-2681082No protein-
 
Retained intron
--TSL:5
ENST00000471848.1CFB-262764No protein-
 
Retained intron
--TSL:2
ENST00000489768.1CFB-269685No protein-
 
Retained intron
--TSL:2
ENST00000468339.1CFB-261589No protein-
 
Retained intron
--TSL:2
ENST00000481293.1CFB-265526No protein-
 
Retained intron
--TSL:2