We define, test, and illustrate use of a range-separated (screened) hybrid, termed vdW-DF2-ahbr and abbreviated AHBR, that uses the second-generation nonlocal-correlation formulation [PRB 82, 081101(R) (2010)] within the van der Waals density functional (vdW-DF) method [ROPP 78, 066501 (2015)]. It supplements the vdW-DF-ahcx [JPCM 34, 025902 (2022)] (abbreviated AHCX) which relies on the first general-geometry formulation of the nonlocal correlation energy [PRL 92, 246401 (2004)]. We build the AHBR off a new analytical-hole analysis of the exchange in vdW-DF2-b86r [PRB 89, 121103 (2014)]. Like AHCX, the AHBR uses an exchange enhancement with a large-gradient behavior that prevents spurious exchange binding and with a small-gradient form that is set from many-body perturbation analysis. Unlike AHCX, however, the AHBR relies on a slightly different interpretation of this input, moving the resulting exchange description closer to PBEsol exchange [PRL 100, 136406 (2008)]. We validate that the range-separated hybrid (RSH) vdW-DF AHBR retains and exceeds the strong AHCX performance both on bulk and in a complete planewave benchmarking across the full GMTKN55 suite on broad molecular properties [PCCP 19, 32184 (2017)]. Interestingly, the AHBR accuracy gains are most pronounced for the class of barrierheights benchmarks, suggesting that the AHBR is evenly robust for transition-state and binding properties. Finally, we show that AHBR correctly predicts DNA base-pair stacking energies, the binding-site preference for CO/Pt(111), and CO2 adsorption in Mg-MOF74.