Google DeepMind has released AlphaGenome Atlas, a catalogue of precomputed predictions for the molecular effects of every possible single-nucleotide variant in the human genome. That is roughly 9 billion single-letter changes. The release also introduces the AlphaGenome Variant Impact (AVI) score, a single number that ranks variants by predicted impact, plus per-variant feature attributions and a genome-wide motif collection. The resource ships as a free web portal for academic use, through the AlphaGenome API, and as a skill in Google Antigravity.
Is it deployable? Partially. The Atlas is queryable today for non-commercial research via the portal and API, and commercial access on Google Cloud is listed as “coming soon”. The underlying AlphaGenome model is already available for academic use on GitHub and for commercial use on Model Garden on Google Cloud.
From one model to a genome-wide map
AlphaGenome, released in June 2025, predicts how a DNA variant changes molecular processes such as gene expression and RNA splicing. It has been used widely, but always one variant or one region at a time. The Atlas changes the unit of work. DeepMind team ran AlphaGenome across all 9 billion single-nucleotide variants and stored the outputs, producing a 1-petabyte dataset. This is more than 30 times larger than the AlphaFold Database, which holds over 200 million protein structure predictions.
