Human (GRCh37.p13)
Description

Fanconi anemia, complementation group B [Source:HGNC Symbol;Acc:3583]

Gene Synonyms

FA2, FAAP90, FAAP95, FAB, FACB, FLJ34064

Location

Chromosome X: 14,861,529-14,891,191 reverse strand.

GRCh37:CM000685.1

About this gene

This gene has 4 transcripts (splice variants) and is associated with 7 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000398334.1FANCB-2013008859aaENSP00000381378.1
 
Protein coding
CCDS14161C9J5X9 Q8NB91 NM_001018113.1GENCODE basic
ENST00000324138.3FANCB-0012894859aaENSP00000326819.3
 
Protein coding
CCDS14161C9J5X9 Q8NB91 NM_152633.2GENCODE basic
ENST00000452869.1FANCB-0022712818aaENSP00000397849.1
 
Protein coding
C9J5X9 -CDS 3' incomplete
ENST00000489126.1FANCB-003559No protein-
 
Retained intron
---