Human (GRCh37.p13)
Description

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

Gene Synonyms

FA2, FAAP90, FAAP95, FAB, FACB, FLJ34064

Location
About this transcript

This transcript has 9 exons, is associated with 8648 variant alleles and maps to 394 oligo probes.

Gene
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
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Statistics

Exons: 9, Coding exons: 8, Transcript length: 2,894 bps, Translation length: 859 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8NB91

CCDS

This transcript is a member of the Human CCDS set: CCDS14161

Version

ENST00000324138.3

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000055835 (version 1)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.