Version 4.77 (#4425)

Clinical-Genomics · Feb 14, 2024 · d3c0549 · d3c0549
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diff --git a/CHANGELOG.md b/CHANGELOG.md
@@ -4,7 +4,7 @@ This project adheres to [Semantic Versioning](http://semver.org/).
 
 About changelog [here](https://keepachangelog.com/en/1.0.0/)
 
-## [unreleased]
+## [4.77]
 ### Added
 - Orpha disease terms now include information on inheritance
 - Case loading via .yaml config file accepts subject_id and phenotype_groups (if previously defined as constant default or added per institute)

diff --git a/scout/__version__.py b/scout/__version__.py
@@ -1 +1 @@
-__version__ = "4.76"
+__version__ = "4.77"