Human (GRCh38.p14)
Description

chymotrypsinogen B2 [Source:HGNC Symbol;Acc:HGNC:2522]

Location

Chromosome 16: 75,204,103-75,207,161 reverse strand.

GRCh38:CM000678.2

View alleles of this gene on alternative sequences

About this gene

This gene has 6 transcripts (splice variants), 1 gene allele, 271 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000303037.13CTRB2-201870263aaENSP00000303963.8
 
Protein coding
CCDS32489Q6GPI1 NM_001025200.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000562387.1CTRB2-204626137aaENSP00000455207.1
 
Protein coding
H3BP92 -TSL:3CDS 5' incomplete
ENST00000562106.5CTRB2-203565168aaENSP00000454599.1
 
Protein coding
H3BMY1 -TSL:3CDS 5' incomplete
ENST00000567767.5CTRB2-206560114aaENSP00000457279.1
 
Protein coding
H3BTQ4 -TSL:5CDS 5' incomplete
ENST00000481611.1CTRB2-2022248No protein-
 
Retained intron
--TSL:2
ENST00000565656.1CTRB2-205581No protein-
 
Retained intron
--TSL:2