Browse a Genome
Ensembl is a genome browser for vertebrate genomes that supports research in comparative genomics, evolution, sequence variation and transcriptional regulation. Ensembl annotate genes, computes multiple alignments, predicts regulatory function and collects disease data. Ensembl tools include BLAST, BLAT, BioMart and the Variant Effect Predictor (VEP) for all supported species.
All genomes
Other species are available in Ensembl Pre! and EnsemblGenomes
Still using GRCh37?
We have a separate site dedicated to the GRCh37 Homo sapiens assembly, with the latest online tools including VEP, Data Slicer, Allele Frequency Calculator and more!
Learn more about how to migrate your data to GRCh38
Find a Data Display
Not sure how to find the data visualisation you need? With our new Find a Data Display page, you can choose a gene, region or variant and then browse a selection of relevant visualisations
What's New in Ensembl Release 89 (May 2017)
- Microarray Probe Mapping Update
- Mouse: update to Ensembl-Havana GENCODE gene set
- Map array probes onto 15 mouse strains
- Beacon endpoint
- Mouse: updated cDNA alignments
Full details | All web updates, by release | More news on our blog
- 06 Jul 2017: GFF3 and Sequence Ontology terms
- 19 Jun 2017: Ensembl Genomes 36 is now live
- 16 Jun 2017: What’s coming in Ensembl release 90
Ensembl creates, integrates and distributes reference datasets and analysis tools that enable genomics. We are based at EMBL-EBI and our software and data are freely available.
Our acknowledgements page includes a list of current and previous funding bodies. How to cite Ensembl in your own publications.
Ensembl release 89 - May 2017 ©
EMBL-EBI
EMBL-EBI
http://asia.ensembl.org
.
Get help
.