Human (GRCh38.p14)
Description

ATPase H+ transporting V1 subunit B2 [Source:HGNC Symbol;Acc:HGNC:854]

Gene Synonyms

ATP6B2, HO57, VATB, VMA2, VPP3

Location

Chromosome 8: 20,197,381-20,226,819 forward strand.

GRCh38:CM000670.2

About this gene

This gene has 6 transcripts (splice variants), 230 orthologues, 4 paralogues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000276390.7ATP6V1B2-2012856511aaENSP00000276390.2
 
Protein coding
CCDS6014A0A140VK65 P21281 NM_001693.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000519667.1ATP6V1B2-202670199aaENSP00000430682.1
 
Protein coding
H0YC04 -TSL:1CDS 5' incomplete
ENST00000521442.1ATP6V1B2-20473849aaENSP00000430866.1
 
Nonsense mediated decay
H0YC45 -TSL:3CDS 5' incomplete
ENST00000520830.1ATP6V1B2-20364956aaENSP00000428069.1
 
Nonsense mediated decay
H0YAT8 -TSL:3CDS 5' incomplete
ENST00000523478.5ATP6V1B2-20557266aaENSP00000430154.1
 
Nonsense mediated decay
E5RGH6 -TSL:4
ENST00000523482.5ATP6V1B2-2066907No protein-
 
Retained intron
--TSL:2