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GENOME AGGREGATION DATABASE

gnomAD v3.1.1gnomAD v2.1.1ExAC


Please note that gnomAD v2.1.1 and v3.1.1 have substantially different but
overlapping sample compositions and are on different genome builds. For more
information, see "Should I switch to the latest version of gnomAD?"

Examples
 * Gene: PCSK9
 * Transcript: ENST00000302118
 * gnomAD v2.1.1 variant: 1-55516888-G-GA
 * gnomAD v3.1.1 variant: 1-55051215-G-GA

The Genome Aggregation Database (gnomAD) is a resource developed by an
international coalition of investigators, with the goal of aggregating and
harmonizing both exome and genome sequencing data from a wide variety of
large-scale sequencing projects, and making summary data available for the wider
scientific community.

The v2.1.1 data set (GRCh37/hg19) provided on this website spans 125,748 exome
sequences and 15,708 whole-genome sequences from unrelated individuals sequenced
as part of various disease-specific and population genetic studies. The v3.1.1
data set (GRCh38) spans 76,156 genomes, selected as in v2. The gnomAD Principal
Investigators and groups that have contributed data to the current release are
listed here.

All data here are released for the benefit of the wider biomedical community,
without restriction on use - see the terms of use. Sign up for our mailing list
for future release announcements.