Upcoming Ensembl Platform Transition

This is the final release of its kind on this website.

In summer 2026, this site will bring you to the new Ensembl platform currently at beta.ensembl.org.
Please bookmark this archive to retain access to the current site, tools and functionality until they are available on the new platform -> jun2026.archive.ensembl.org

 
Ensembl Home
More ▼
Search »
In this section

SNPs and other variants for my gene

Variation Table

Find short variants for a gene from dbSNP, COSMIC, and other sources in the Gene Variation table.

Since this table can contain many variants, we suggest filtering by consequence type.

[Click to enlarge]

Find out more:

Gene sequence

View variants within the nucleotide sequence in the Gene Sequence view.

[Click to enlarge]

Find out more:

In all views, click on any Variant to find population frequencies, alleles, and more in the variation tab.

Find out more:

Variants along the genome

View variants along the genome in the Location tab. Choose different types and sources, for example 1000 Genomes populations, ClinVar (clinically associated), OMIM and HGMD (public set).

[Click to enlarge]

Find out more:

You can also browse SNPs throughout the genome - find out how in this video: