Human (GRCh38.p14)
Description

HNF1 homeobox B [Source:HGNC Symbol;Acc:HGNC:11630]

Gene Synonyms

HNF1B, HNF1BETA, LFB3, MODY5, TCF2, VHNF1

Location

Scaffold HSCHR17_7_CTG4: 1,925,499-1,984,303 reverse strand.

GRCh38:KI270857.1

View this gene on the primary assembly.

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000610754.4HNF1B-2062978557aaENSP00000484591.1
 
Protein coding
P35680-1 -Ensembl CanonicalGENCODE basicTSL:1
ENST00000633792.1HNF1B-2111971531aaENSP00000488080.1
 
Protein coding
P35680-2 -GENCODE basicTSL:1
ENST00000616941.3HNF1B-2081820425aaENSP00000484132.1
 
Protein coding
E0YMJ8 -GENCODE basicTSL:1
ENST00000632625.1HNF1B-2101819548aaENSP00000488519.1
 
Protein coding
A0A087WZC2 -GENCODE basicTSL:5
ENST00000614955.4HNF1B-2071546457aaENSP00000479629.1
 
Protein coding
A0A0C4DGS8 -GENCODE basicTSL:1
ENST00000619478.2HNF1B-2091103293aaENSP00000481082.1
 
Protein coding
A0A087WXS2 -GENCODE basicTSL:5
ENST00000633873.1HNF1B-2123481No protein-
 
Retained intron
--TSL:2