Previous studies have demonstrated that the immunoglobulin G (IgG) N-glycome and transcriptome are potential biochemical signatures of chronological and biological ages, and several aging clocks have been developed. By integrating the IgG N-glycome and transcriptome, we propose a novel aging clock, gtAge. We developed a deep reinforcement learning-based multiomics integration method called AlphaSnake. The results showed that AlphaSnake achieved a predicted coefficient of determination (R2) value of 0.853, outperforming the concatenation-based integration method (R2 = 0.820) The gtAge estimated by AlphaSnake explained up to 85.3% of the variance in chronological age, which was higher than that in age predicted from IgG N-glycome solely (gAge; R2 = 0.290) and age predicted from transcriptome solely (tAge; R2 = 0.812). We also found that the delta age—the difference between the predicted age and chronological age—was associated with several age-related phenotypes. Both delta gtAge and tAge were negatively associated with high-density lipoprotein (p = 0.02 and p = 0.022, respectively), whereas delta gAge was positively correlated with cholesterol (p = 0.006), triglyceride (p = 0.002), fasting plasma glucose (p = 0.014), low-density lipoprotein (p = 0.006), and glycated hemoglobin (p = 0.039). These findings suggest that gtAge, tAge, and gAge are potential biomarkers for biological age.